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FDA 510(k), K120033, ACTIVAC THERAPY UNIT AND INFOVAC THERAPY UNIT, VAC ATS THERAPY UNIT AND VAC FREEDOM THERAPY UNIT, VAC VIA THERAPY UNIT
FDA 510(k), K120033, ACTIVAC THERAPY UNIT AND INFOVAC THERAPY UNIT, VAC ATS THERAPY UNIT AND VAC FREEDOM THERAPY UNIT, VAC VIA THERAPY UNIT
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510(K) Number: K120033
Device Name: ACTIVAC THERAPY UNIT AND INFOVAC THERAPY UNIT, VAC ATS THERAPY UNIT AND VAC FREEDOM THERAPY UNIT, VAC VIA THERAPY UNIT
Manufacturer: KCI USA, INC.
Device Classification Name: Negative Pressure Wound Therapy Powered Suction Pump
Regulation Number: 878.4780
Classification Product Code: OMP
Date Received: 01/04/2012
Decision Date: 05/31/2012
Regulation Medical Specialty: General & Plastic Surgery
Device Name: ACTIVAC THERAPY UNIT AND INFOVAC THERAPY UNIT, VAC ATS THERAPY UNIT AND VAC FREEDOM THERAPY UNIT, VAC VIA THERAPY UNIT
Manufacturer: KCI USA, INC.
Device Classification Name: Negative Pressure Wound Therapy Powered Suction Pump
Regulation Number: 878.4780
Classification Product Code: OMP
Date Received: 01/04/2012
Decision Date: 05/31/2012
Regulation Medical Specialty: General & Plastic Surgery
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- Delivery: Approximately 1 to 2 weeks
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