HHS - 21 CFR PART 803
MEDICAL DEVICE REPORTING
active, Most Current
| Organization: | HHS |
| Publication Date: | 1 April 2022 |
| Status: | active |
| Page Count: | 18 |
Document History
April 1, 2023
MEDICAL DEVICE REPORTING
A description is not available for this item.
21 CFR PART 803
April 1, 2022
MEDICAL DEVICE REPORTING
A description is not available for this item.
April 1, 2021
MEDICAL DEVICE REPORTING
A description is not available for this item.
April 1, 2019
MEDICAL DEVICE REPORTING
A description is not available for this item.
April 1, 2018
MEDICAL DEVICE REPORTING
What does this part cover?
(a) This part establishes the requirements for medical device reporting for device user facilities, manufacturers, importers, and distributors. If you are a device user...
April 1, 2017
MEDICAL DEVICE REPORTING
A—General Provisions
What does this part cover?
(a) This part establishes the requirements for medical device reporting for device user facilities, manufacturers, importers, and distributors. If...
April 1, 2016
MEDICAL DEVICE REPORTING
What does this part cover?
(a) This part establishes the requirements for medical device reporting for device user facilities, manufacturers, importers, and distributors. If you are a device user...
April 1, 2015
MEDICAL DEVICE REPORTING; (Eff. Until 8-14-15)
What does this part cover?
(a) This part establishes the requirements for medical device reporting for device user facilities, manufacturers, importers, and distributors. If you are a device user...
April 1, 2014
MEDICAL DEVICE REPORTING; (Eff. Until 8-14-15)
What does this part cover?
(a) This part establishes the requirements for medical device reporting for device user facilities, manufacturers, importers, and distributors. If you are a device user...