K-number	K962119
Device name	RE-NEW LAPAROSCOPIC INSTRUMENTS
Applicant	Microline Pentax, Inc.
Product code	GEI
Device class	Class II
Decision date	Aug 9, 1996
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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RE-NEW LAPAROSCOPIC INSTRUMENTS

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