REPROCESSED HARMONIC SCALPEL— 510(k) K083060

Substantially Equivalent

Sterilmed, Inc.

FDA 510(k) clearance K083060 for REPROCESSED HARMONIC SCALPEL, Substantially Equivalent on 2009-01-09. Applicant: Sterilmed, Inc..

Clearance details

Applicant: Sterilmed, Inc.
Product code: Code NLQ
Advisory panel: Unknown
Date received: 2008-10-14
Decision date: 2009-01-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Maple Grove, MN, US

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