FDA 510(k), K143014, F5
FDA 510(k), K143014, F5
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$149.00 USD
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510(K) Number: K143014
Device Name: F5
Manufacturer: PERMOBIL AB
Device Classification Name: wheelchair, powered
Regulation Number: 890.3860
Classification Product Code: ITI
Date Received: 10/20/2014
Decision Date: 03/25/2015
Regulation Medical Specialty: Physical Medicine
Device Name: F5
Manufacturer: PERMOBIL AB
Device Classification Name: wheelchair, powered
Regulation Number: 890.3860
Classification Product Code: ITI
Date Received: 10/20/2014
Decision Date: 03/25/2015
Regulation Medical Specialty: Physical Medicine