K-number	K970317
Device name	MODIFIED E-PACK PROCEDURE KIT
Applicant	ETHICON, Inc.
Product code	GAM
Device class	Class II
Decision date	Apr 25, 1997
Decision	Substantially Equivalent
Regulation	878.4493

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View the full FDA submission: accessdata.fda.gov

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MODIFIED E-PACK PROCEDURE KIT

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