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FDA 510(k), K030427, HP-3 HD ELECTRIC WHEELCHAIR
FDA 510(k), K030427, HP-3 HD ELECTRIC WHEELCHAIR
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$149.00 USD
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510(K) Number: K030427
Device Name: HP-3 HD ELECTRIC WHEELCHAIR
Manufacturer: IMC-HEARTWAY, LLC
Device Classification Name: wheelchair, powered
Regulation Number: 890.3860
Classification Product Code: ITI
Date Received: 02/10/2003
Decision Date: 04/18/2003
Regulation Medical Specialty: Physical Medicine
Device Name: HP-3 HD ELECTRIC WHEELCHAIR
Manufacturer: IMC-HEARTWAY, LLC
Device Classification Name: wheelchair, powered
Regulation Number: 890.3860
Classification Product Code: ITI
Date Received: 02/10/2003
Decision Date: 04/18/2003
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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