K-number	K930666
Device name	REUSABLE LAPAROSCOPIC INSTRUMENTS W/ ELECTROCAUTERY
Applicant	Snowden-Pencer
Product code	GEI
Device class	Class II
Decision date	May 19, 1994
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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REUSABLE LAPAROSCOPIC INSTRUMENTS W/ ELECTROCAUTERY

Everything you need for a 510(k) submission. Nothing you don't.