K-number	K012598
Device name	REPROCESSED LAPAROSCOPIC ELECTRIC INSTUMENTS
Applicant	Sterilmed, Inc.
Product code	NUJ
Device class	Class II
Decision date	Nov 7, 2001
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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REPROCESSED LAPAROSCOPIC ELECTRIC INSTUMENTS

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