K-number	K182838
Device name	Geistlich Derma-Gide
Applicant	Geistlich Pharma AG
Product code	KGN
Device class	Class U
Decision date	Nov 8, 2018
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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Geistlich Derma-Gide

Everything you need for a 510(k) submission. Nothing you don't.