K-number	K970159
Device name	FLEX-NECK PD CATHETER
Applicant	Janin Group, Inc.
Product code	FJS
Device class	Class II
Decision date	Sep 5, 1997
Decision	Substantially Equivalent
Regulation	876.5630

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View the full FDA submission: accessdata.fda.gov

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FLEX-NECK PD CATHETER

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