FDA 510(k), K993455, FLIPPER DETACHABLE EMBOLIZATION COIL

FDA 510(k), K993455, FLIPPER DETACHABLE EMBOLIZATION COIL

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510(K) Number: K993455
Device Name: FLIPPER DETACHABLE EMBOLIZATION COIL
Manufacturer: KAREN BRADBURN
Device Classification Name: Device, Vascular, For Promoting Embolization
Regulation Number: KRD
Classification Product Code: 10/13/1999
Date Received: 01/11/2000
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
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