HHS - 21 CFR PART 803
MEDICAL DEVICE REPORTING
active, Most Current
| Organization: | HHS |
| Publication Date: | 1 April 2019 |
| Status: | active |
| Page Count: | 18 |
Document History
21 CFR PART 803
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...