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FDA 510(k), K011208, BIOVER
FDA 510(k), K011208, BIOVER
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510(K) Number: K011208
Device Name: BIOVER
Manufacturer: BIOVER AG
Device Classification Name: Clamp, Vascular
Regulation Number: 870.4450
Classification Product Code: DXC
Date Received: 04/19/2001
Decision Date: 10/02/2002
Regulation Medical Specialty: Cardiovascular
Device Name: BIOVER
Manufacturer: BIOVER AG
Device Classification Name: Clamp, Vascular
Regulation Number: 870.4450
Classification Product Code: DXC
Date Received: 04/19/2001
Decision Date: 10/02/2002
Regulation Medical Specialty: Cardiovascular
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