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FDA 510(k), K103122, C-MAX, C-MAX U1, C-MAX U1 160KG, C-MAX U2, C-MAX U2 160KG, S-MAX, S-MAX AVIATION, S-MAX SELLA, S-MAX SELLA 160KG
FDA 510(k), K103122, C-MAX, C-MAX U1, C-MAX U1 160KG, C-MAX U2, C-MAX U2 160KG, S-MAX, S-MAX AVIATION, S-MAX SELLA, S-MAX SELLA 160KG
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510(K) Number: K103122
Device Name: C-MAX, C-MAX U1, C-MAX U1 160KG, C-MAX U2, C-MAX U2 160KG, S-MAX, S-MAX AVIATION, S-MAX SELLA, S-MAX SELLA 160KG
Manufacturer: AAT ALBER ANTRIEBSTECHNIK GMBH
Device Classification Name: transport, patient, powered
Regulation Number: 890.5150
Classification Product Code: ILK
Date Received: 10/21/2010
Decision Date: 12/30/2010
Regulation Medical Specialty: Physical Medicine
Device Name: C-MAX, C-MAX U1, C-MAX U1 160KG, C-MAX U2, C-MAX U2 160KG, S-MAX, S-MAX AVIATION, S-MAX SELLA, S-MAX SELLA 160KG
Manufacturer: AAT ALBER ANTRIEBSTECHNIK GMBH
Device Classification Name: transport, patient, powered
Regulation Number: 890.5150
Classification Product Code: ILK
Date Received: 10/21/2010
Decision Date: 12/30/2010
Regulation Medical Specialty: Physical Medicine
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