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FDA 510(k), K990358, CROSS SPORT, RIGID WHEELCHAIR
FDA 510(k), K990358, CROSS SPORT, RIGID WHEELCHAIR
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510(K) Number: K990358
Device Name: CROSS SPORT, RIGID WHEELCHAIR
Manufacturer: TISPORT
Device Classification Name: Wheelchair, Mechanical
Regulation Number: 890.3850
Classification Product Code: IOR
Date Received: 02/05/1999
Decision Date: 02/26/1999
Regulation Medical Specialty: Physical Medicine
Device Name: CROSS SPORT, RIGID WHEELCHAIR
Manufacturer: TISPORT
Device Classification Name: Wheelchair, Mechanical
Regulation Number: 890.3850
Classification Product Code: IOR
Date Received: 02/05/1999
Decision Date: 02/26/1999
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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