CFR 21-801 - Labeling

From knowledgebase
Revision as of 07:18, 25 August 2020 by Dirkjan (talk | contribs) (Created page with "These regulations implement FDA's responsibility for and authority over each medical device's labeling. Labeling inclues all labels and other written, printed, or graphic matt...")
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigation Jump to search

These regulations implement FDA's responsibility for and authority over each medical device's labeling. Labeling inclues all labels and other written, printed, or graphic matter on any device or its containers or wrappers or accompanying such devices and includes advertising matter and oral or written statements made by manufacturers or their representatives.