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FDA 510(k), K151199, SmartDrive Wheelchair Power Assist
FDA 510(k), K151199, SmartDrive Wheelchair Power Assist
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510(K) Number: K151199
Device Name: SmartDrive Wheelchair Power Assist
Manufacturer: MAX MOBILITY, LLC
Device Classification Name: wheelchair, powered
Regulation Number: 890.3860
Classification Product Code: ITI
Date Received: 05/05/2015
Decision Date: 07/30/2015
Regulation Medical Specialty: Physical Medicine
Device Name: SmartDrive Wheelchair Power Assist
Manufacturer: MAX MOBILITY, LLC
Device Classification Name: wheelchair, powered
Regulation Number: 890.3860
Classification Product Code: ITI
Date Received: 05/05/2015
Decision Date: 07/30/2015
Regulation Medical Specialty: Physical Medicine
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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