FDA 510(k), K090094, ZELTIQ SYSTEM
FDA 510(k), K090094, ZELTIQ SYSTEM
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$149.00 USD
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$149.00 USD
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510(K) Number: K090094
Device Name: ZELTIQ SYSTEM
Manufacturer:
Device Classification Name: Powered Laser Surgical Instrument
Regulation Number: 878.4810
Classification Product Code: GEX
Date Received: 01/14/2009
Decision Date: 05/20/2009
Regulation Medical Specialty: General & Plastic Surgery
Device Name: ZELTIQ SYSTEM
Manufacturer:
Device Classification Name: Powered Laser Surgical Instrument
Regulation Number: 878.4810
Classification Product Code: GEX
Date Received: 01/14/2009
Decision Date: 05/20/2009
Regulation Medical Specialty: General & Plastic Surgery