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FDA 510(k), K130864, C-MAX+ (PLUS)
FDA 510(k), K130864, C-MAX+ (PLUS)
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$149.00 USD
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510(K) Number: K130864
Device Name: C-MAX+ (PLUS)
Manufacturer: AAT ALBER ANTRIEBSTECHNIK GMBH
Device Classification Name: Transport, Patient, Powered
Regulation Number: 890.5150
Classification Product Code: ILK
Date Received: 03/28/2013
Decision Date: 02/06/2014
Regulation Medical Specialty: Physical Medicine
Device Name: C-MAX+ (PLUS)
Manufacturer: AAT ALBER ANTRIEBSTECHNIK GMBH
Device Classification Name: Transport, Patient, Powered
Regulation Number: 890.5150
Classification Product Code: ILK
Date Received: 03/28/2013
Decision Date: 02/06/2014
Regulation Medical Specialty: Physical Medicine
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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