FDA 510(k), K100384, FIBERLASE C02 LASER WAVEGUIDE
FDA 510(k), K100384, FIBERLASE C02 LASER WAVEGUIDE
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$149.00 USD
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$149.00 USD
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510(K) Number: K100384
Device Name: FIBERLASE C02 LASER WAVEGUIDE
Manufacturer: AHAVA STEIN
Device Classification Name: Powered Laser Surgical Instrument
Regulation Number: GEX
Classification Product Code: 02/16/2010
Date Received: 04/12/2010
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: FIBERLASE C02 LASER WAVEGUIDE
Manufacturer: AHAVA STEIN
Device Classification Name: Powered Laser Surgical Instrument
Regulation Number: GEX
Classification Product Code: 02/16/2010
Date Received: 04/12/2010
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery