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HHS - 21 CFR PART 1020

PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS

active, Most Current
Organization: HHS
Publication Date: 1 April 2022
Status: active
Page Count: 33

Document History

21 CFR PART 1020
April 1, 2022
PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
A description is not available for this item.
21 CFR PART 1020
April 1, 2021
PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
A description is not available for this item.
21 CFR PART 1020
April 1, 2020
PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
A description is not available for this item.
21 CFR PART 1020
April 1, 2019
PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
A description is not available for this item.
21 CFR PART 1020
April 1, 2018
PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
Applicability. The provisions of this section are applicable to television receivers manufactured subsequent to January 15, 1970
21 CFR PART 1020
April 1, 2017
PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
A description is not available for this item.
21 CFR PART 1020
April 1, 2016
PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
Applicability. The provisions of this section are applicable to television receivers manufactured subsequent to January 15, 1970.
21 CFR PART 1020
April 1, 2015
PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
A description is not available for this item.
21 CFR PART 1020
April 1, 2014
PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
A description is not available for this item.
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References

This document is referenced by:
AAMI 60601-1-2 - MEDICAL ELECTRICAL EQUIPMENT – Part 1-2: General requirements for basic safety and essential performance – Collateral Standard: Electromagnetic disturbances – Requirements and tests
Published by AAMI on January 1, 2014
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS....
This document is referenced by:
EN IEC 60601-2-43 - Medical electrical equipment - Part 2-43: Particular requirements for the basic safety and essential performance of X-ray equipment for interventional procedures
Published by CENELEC on January 1, 2023
This document applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of both FIXED and MOBILE X-RAY EQUIPMENT declared by the MANUFACTURER to be suitable for RADIOSCOPICALLY GUIDED INTERVENTIONAL...
This document is referenced by:
NEN-EN-IEC 60601-2-43 - Medical electrical equipment - Part 2-43: Particular requirements for the basic safety and essential performance of X-ray equipment for interventional procedures
Published by NEN on February 1, 2023
This document applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of both FIXED and MOBILE X-RAY EQUIPMENT declared by the MANUFACTURER to be suitable for RADIOSCOPICALLY GUIDED INTERVENTIONAL...
This document is referenced by:
AR 750-1 - Army Materiel Maintenance Policy
Published by ARMY on February 2, 2023
Purpose This regulation establishes policies and assigns responsibilities for the maintenance of Army materiel. It provides and defines requirements for performance and management of the materiel...
This document is referenced by:
ASTM F3107 - Standard Test Method for Measuring Accuracy after Mechanical Disturbances on Reference Frames of Computer Assisted Surgery Systems
Published by ASTM on December 1, 2014
This standard will measure the effects on the accuracy of computer assisted surgery (CAS) systems of the environmental influences caused by equipment utilized for bone preparation during the intended...
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