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FDA 510(k), K082391, PRIMAEVA MEDICAL RENESIS SYSTEM
FDA 510(k), K082391, PRIMAEVA MEDICAL RENESIS SYSTEM
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$149.00 USD
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$149.00 USD
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510(K) Number: K082391
Device Name: PRIMAEVA MEDICAL RENESIS SYSTEM
Manufacturer:
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 08/19/2008
Decision Date: 09/01/2009
Regulation Medical Specialty: General & Plastic Surgery
Device Name: PRIMAEVA MEDICAL RENESIS SYSTEM
Manufacturer:
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 08/19/2008
Decision Date: 09/01/2009
Regulation Medical Specialty: General & Plastic Surgery
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