K-number	K771529
Device name	PERITONEAL INTRODUCER & SHEATH
Applicant	Cordis Corp.
Product code	GYK
Device class	Class I
Decision date	Aug 16, 1977
Decision	Substantially Equivalent
Regulation	882.4545

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View the full FDA submission: accessdata.fda.gov

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PERITONEAL INTRODUCER & SHEATH

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