REPROCESSED LAPAROSCOPIC ELECTRIC INSTUMENTS— 510(k) K012598

Substantially Equivalent

Sterilmed, Inc.

FDA 510(k) clearance K012598 for REPROCESSED LAPAROSCOPIC ELECTRIC INSTUMENTS, Substantially Equivalent on 2001-11-07. Applicant: Sterilmed, Inc..

Clearance details

Applicant: Sterilmed, Inc.
Product code: Code NUJ
Advisory panel: General, Plastic Surgery
Date received: 2001-08-10
Decision date: 2001-11-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Maple Grove, MN, US

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