K-number	K920289
Device name	CORDIS BIPAL 7 BIOPSY FORCEPS
Applicant	Cordis Corp.
Product code	DWZ
Device class	Class II
Decision date	Mar 30, 1992
Decision	Substantially Equivalent
Regulation	870.4075

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View the full FDA submission: accessdata.fda.gov

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CORDIS BIPAL 7 BIOPSY FORCEPS

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