FDA 510(k), K133718, ZERONA

FDA 510(k), K133718, ZERONA

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510(K) Number: K133718
Device Name: ZERONA
Manufacturer: ERCHONIA CORPORATION
Device Classification Name: fat reducing low level laser
Regulation Number: 878.5400
Classification Product Code: OLI
Date Received: 12/04/2013
Decision Date: 05/12/2014
Regulation Medical Specialty: General & Plastic Surgery

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