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

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