K-number	K032847
Device name	EXCISOR BIOPTOME, MODEL 01-0004
Applicant	Acueity, Inc.
Product code	KNW
Device class	Class II
Decision date	Sep 26, 2003
Decision	Substantially Equivalent
Regulation	876.1075

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View the full FDA submission: accessdata.fda.gov

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EXCISOR BIOPTOME, MODEL 01-0004

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