K-number	K892691
Device name	CATHETERS, MALE, FEMALE
Applicant	Zinnanti Surgical Instruments, Inc.
Product code	KOD
Device class	Class II
Decision date	Jun 23, 1989
Decision	Substantially Equivalent
Regulation	876.5130

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View the full FDA submission: accessdata.fda.gov

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CATHETERS, MALE, FEMALE

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