K-number	K921833
Device name	ENDOPATH ENDO-SURGERY PERCUTANEOUS CATHETER INTROD
Applicant	ETHICON, Inc.
Product code	FMF
Device class	Class II
Decision date	Sep 21, 1992
Decision	Unknown
Regulation	880.5860

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View the full FDA submission: accessdata.fda.gov

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ENDOPATH ENDO-SURGERY PERCUTANEOUS CATHETER INTROD

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