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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...

References

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