REPROCESSED VESSEL SEALER— 510(k) K123096

Substantially Equivalent

Sterilmed, Inc.

FDA 510(k) clearance K123096 for REPROCESSED VESSEL SEALER, Substantially Equivalent on 2013-01-25. Applicant: Sterilmed, Inc..

Clearance details

Applicant: Sterilmed, Inc.
Product code: Code NUJ
Advisory panel: General, Plastic Surgery
Date received: 2012-10-02
Decision date: 2013-01-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Maple Grove, MN, US

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