FDA 510(k), K082586, LIGHTWAVE PROFESSIONAL DELUXE
FDA 510(k), K082586, LIGHTWAVE PROFESSIONAL DELUXE
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$149.00 USD
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$149.00 USD
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510(K) Number: K082586
Device Name: LIGHTWAVE PROFESSIONAL DELUXE
Manufacturer:
Device Classification Name: Powered Laser Surgical Instrument
Regulation Number: 878.4810
Classification Product Code: GEX
Date Received: 09/08/2008
Decision Date: 01/04/2010
Regulation Medical Specialty: General & Plastic Surgery
Device Name: LIGHTWAVE PROFESSIONAL DELUXE
Manufacturer:
Device Classification Name: Powered Laser Surgical Instrument
Regulation Number: 878.4810
Classification Product Code: GEX
Date Received: 09/08/2008
Decision Date: 01/04/2010
Regulation Medical Specialty: General & Plastic Surgery