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FDA 510(k), K041219, ELECTRO
FDA 510(k), K041219, ELECTRO
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510(K) Number: K041219
Device Name: ELECTRO
Manufacturer: PERMOBIL A.B.
Device Classification Name: wheelchair, powered
Regulation Number: 890.3860
Classification Product Code: ITI
Date Received: 05/10/2004
Decision Date: 08/04/2004
Regulation Medical Specialty: Physical Medicine
Device Name: ELECTRO
Manufacturer: PERMOBIL A.B.
Device Classification Name: wheelchair, powered
Regulation Number: 890.3860
Classification Product Code: ITI
Date Received: 05/10/2004
Decision Date: 08/04/2004
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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