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Medical Device Reporting

fda-device · Food and Drug Administration · Rule · Published 2006-01-10 · Effective 2006-01-10 · 71 FR 1488

Document

Document number
06-172
Federal Register citation
71 FR 1488
CFR reference
21 CFR 803
Type
Rule
Action
Final rule; technical amendment.
Category
fda-device
Sub-agency
Food and Drug Administration
Publication date
2006-01-10
Effective date
2006-01-10

Abstract

The Food and Drug Administration (FDA) is amending its medical device reporting regulations to reflect a change in address for agency contacts for reporting a public health emergency. This action is editorial in nature and is intended to improve the accuracy of the agency's regulations.

Source

Authoritative
Federal Register document
Machine
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