K-number	K033593
Device name	REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS
Applicant	Clearmedical, Inc.
Product code	NLU
Device class	Class II
Decision date	Nov 20, 2003
Decision	Substantially Equivalent
Regulation	876.4300

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View the full FDA submission: accessdata.fda.gov

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REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS

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