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pdfDEPARTMENT OF HEALTH AND HUMAN SERVICES
FOOD AND DRUG ADMINISTRATION
Distribution List:
Purchaser
Assembler
State Radiation Health Office
Form Approved: OMB No. 0910-0025
Expiration Date: August 31, 2023
See Reverse for PRA statement
Assembler/Purchaser Control Number
REPORT OF ASSEMBLY
OF A DIAGNOSTIC X-RAY SYSTEM
1. EQUIPMENT LOCATION
2. ASSEMBLER INFORMATION
a. NAME OF HOSPITAL, DOCTOR OR OFFICE WHERE INSTALLED
a. COMPANY NAME
b. STREET ADDRESS
b. STREET ADDRESS
c. CITY
d. STATE
e. ZIP CODE
c. CITY
f. TELEPHONE NUMBER
d. STATE
e. ZIP CODE
f. TELEPHONE NUMBER
3. GENERAL INFORMATION
a. THIS REPORT IS FOR ASSEMBLY OF CERTIFIED COMPONENTS WHICH ARE (Check appropriate box(es))
REASSEMBLY - MIXED SYSTEM (Both certified and non-certified components)
NEW ASSEMBLY - FULLY CERTIFIED SYSTEM
REPLACEMENT COMPONENTS IN AN EXISTING SYSTEM
REASSEMBLY - FULLY CERTIFIED SYSTEM
AN ADDITION TO AN EXISTING SYSTEM
b. INTENDED USE(S) (Check appropriate box(s))
GENERAL PURPOSE RADIOGRAPHY
UROLOGY
CT WHOLE BODY SCANNER
RADIATION THERAPY SIMULATOR
GENERAL PURPOSE FLUOROSCOPY
MAMMOGRAPHY
HEAD-NECK (Medical)
C-ARM FLUOROSCOPIC
TOMOGRAPHY (Other than CT)
CHEST
DENTAL-INTRAORAL
DIGITAL
ANGIOGRAPHY
CHIROPRACTIC
DENTAL-CEPHALOMETRIC
BONE MINERAL ANALYSIS
PODIATRY
CT HEADSCANNER
DENTAL PANORAMIC
c. THE X-RAY SYSTEM IS (Check one)
OTHER
(Specify in comments)
DENTAL-CT
d. THE MASTER CONTROL IS IN ROOM
e. DATE OF ASSEMBLY
STATIONARY
MOBILE
(mm)
(dd)
(yyyy)
4. COMPONENT INFORMATION (If additional space is needed for this section use another form, replacing the preprinted number with
this Form Number, and complete Items 1, 4, and 5 only)
a. THE MASTER CONTROL IS
b. CONTROL MANUFACTURER
d. CONTROL SERIAL NUMBER
e. DATE MANUFACTURED
A NEW INSTALLATION
EXISTING (Certified)
f. SYSTEM MODEL NAME (CT Systems Only)
c. CONTROL MODEL NUMBER
EXISTING (Non-certified)
Complete the following information for the certified components listed below which you installed. For beam limiting devices, tables and CT gantries enter the manufacturer and Model number in the indicated spaces.
For other certified components, enter in the appropriate blocks how many of each you installed in this system.
g.
h.
SELECTED COMPONENTS
MANUFACTURER
MODEL NUMBER
DATE MANUFACTURED
MANUFACTURER
MODEL NUMBER
DATE MANUFACTURED
OTHER CERTIFIED COMPONENTS
(Enter number of each installed in appropriate blocks.)
X-RAY CONTROL
CRADLE
HIGH VOLTAGE GENERATOR
FILM CHANGER
VERTICAL CASSETTE HOLDER
MANUFACTURER
MODEL NUMBER
DATE MANUFACTURED
IMAGE INTENSIFIER
TUBE HOUSING ASSEMBLY
SPOT FILM DEVICE
DENTAL TUBE HEAD
MANUFACTURER
MODEL NUMBER
MANUFACTURER
MODEL NUMBER
CEPHALOMETRIC DEVICE
FLUOROSCOPIC IMAGING
ASSEMBLY
IMAGE RECEPTOR SUPPORT DEVICE
IMAGE RECEPTOR
OTHER
FLUOROSCOPIC AIR
KERMA DISPLAY DEVICE
DATE MANUFACTURED
DATE MANUFACTURED
5. ASSEMBLER CERTIFICATION
I affirm that all certified components assembled or installed by me, for which this report is being made, were adjusted and tested by me according to the instructions provided by the manufacture(s), were of the type
required by the manufacturer(s), were of the type required by the diagnostic x-ray performance standard (21 CFR Part 1020), were not modified to adversely affect performance, and were installed in accordance with
provisions of 21 CFR Part 1020. I also affirm that all instruction manuals and other information required by 21 CFR Part 1020 for this assembly have been furnished to the purchaser and, within 15 days following
completion of the assembly, a copy of this form will be submitted to the purchaser and, where applicable, to the State agency responsible for radiation protection.
a. PRINTED NAME
b. SIGNATURE
6. COMMENTS
FORM FDA 2579 (12/22)
PREVIOUS EDITIONS MAY BE USED
Contact Information for State Radiation Health Offices is available on the website of the Conference of Radiation Control Program Directors (CRCPD), https://www.crcpd.org/mpage/Map
Form may be downloaded at: https://www.fda.gov/media/144454/download
EF
Contact Information for State Radiation Health Offices is available on the website
of the Conference of Radiation Control Program Directors (CRCPD),
https://www.crcpd.org/mpage/Map
Form may be downloaded at: https://www.fda.gov/media/144454/download
This section applies only to requirements of the Paperwork Reduction Act of 1995.
*DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.*
The burden time for this collection of information is estimated to average 18 minutes per response, including the
time to review instructions, search existing data sources, gather and maintain the data needed and complete
and review the collection of information. Send comments regarding this burden estimate or any other aspect of
this information collection, including suggestions for reducing this burden, to:
Department of Health and Human Services
Food and Drug Administration
Office of Chief Information Officer
Paperwork Reduction Act (PRA) Staff
PRAStaff@fda.hhs.gov
“An agency may not conduct or sponsor, and a person is not required to respond to, a collection of
information unless it displays a currently valid OMB number.”
FORM FDA 2579 (12/22)
PREVIOUS EDITIONS MAY BE USED
File Type | application/pdf |
File Title | FDA Form 2579 |
Subject | Report of Assembly of a Diagnostic X-Ray System |
Author | FDA |
File Modified | 2022-12-12 |
File Created | 2022-12-12 |