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FDA 510(k), K053451, LIPOSAT (INFILTRATION PUMP), MODEL 00 002 274; VACUSAT (SUCTION UNIT), MODEL 00 002 252 (220 V), 00 002 318 (110 V);
FDA 510(k), K053451, LIPOSAT (INFILTRATION PUMP), MODEL 00 002 274; VACUSAT (SUCTION UNIT), MODEL 00 002 252 (220 V), 00 002 318 (110 V);
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510(K) Number: K053451
Device Name: LIPOSAT (INFILTRATION PUMP), MODEL 00 002 274; VACUSAT (SUCTION UNIT), MODEL 00 002 252 (220 V), 00 002 318 (110 V);
Manufacturer: MOELLER MEDICAL GMBH & CO. KG
Device Classification Name: system, suction, lipoplasty for removal
Regulation Number: 878.5040
Classification Product Code: QPB
Date Received: 12/12/2005
Decision Date: 08/25/2006
Regulation Medical Specialty: General & Plastic Surgery
Device Name: LIPOSAT (INFILTRATION PUMP), MODEL 00 002 274; VACUSAT (SUCTION UNIT), MODEL 00 002 252 (220 V), 00 002 318 (110 V);
Manufacturer: MOELLER MEDICAL GMBH & CO. KG
Device Classification Name: system, suction, lipoplasty for removal
Regulation Number: 878.5040
Classification Product Code: QPB
Date Received: 12/12/2005
Decision Date: 08/25/2006
Regulation Medical Specialty: General & Plastic Surgery
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