FDA 510(k), K032123, SHOCKWAVE SUSPENSION WHEELCHAIR
FDA 510(k), K032123, SHOCKWAVE SUSPENSION WHEELCHAIR
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510(K) Number: K032123
Device Name: SHOCKWAVE SUSPENSION WHEELCHAIR
Manufacturer: PER4MAX MEDICAL, LLC
Device Classification Name: wheelchair, mechanical
Regulation Number: 890.3850
Classification Product Code: IOR
Date Received: 07/10/2003
Decision Date: 07/31/2003
Regulation Medical Specialty: Physical Medicine
Device Name: SHOCKWAVE SUSPENSION WHEELCHAIR
Manufacturer: PER4MAX MEDICAL, LLC
Device Classification Name: wheelchair, mechanical
Regulation Number: 890.3850
Classification Product Code: IOR
Date Received: 07/10/2003
Decision Date: 07/31/2003
Regulation Medical Specialty: Physical Medicine
- 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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