SONATHERM 600I ULTRASONIC LESION GENERATING SYSTEM— 510(k) K070779

Substantially Equivalent

Misonix, Inc.

FDA 510(k) clearance K070779 for SONATHERM 600I ULTRASONIC LESION GENERATING SYSTEM, Substantially Equivalent on 2008-07-09. Applicant: Misonix, Inc..

Clearance details

Applicant: Misonix, Inc.
Product code: Code NTB
Advisory panel: General, Plastic Surgery
Date received: 2007-03-21
Decision date: 2008-07-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Farmingdale, NY, US

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