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FDA 510(k), K812639, UNICUFF
FDA 510(k), K812639, UNICUFF
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510(K) Number: K812639
Device Name: UNICUFF
Manufacturer: FRONTIER PRODUCTS
Device Classification Name: transducer, vessel occlusion
Regulation Number: 870.2890
Classification Product Code: DXP
Date Received: 09/16/1981
Decision Date: 10/02/1981
Regulation Medical Specialty: Cardiovascular
Device Name: UNICUFF
Manufacturer: FRONTIER PRODUCTS
Device Classification Name: transducer, vessel occlusion
Regulation Number: 870.2890
Classification Product Code: DXP
Date Received: 09/16/1981
Decision Date: 10/02/1981
Regulation Medical Specialty: Cardiovascular
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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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