FDA 510(k), K083091, LC BEAD MICROSPHERES, BEAD BLOCK COMPRESSIBLE MICROSPHERES

FDA 510(k), K083091, LC BEAD MICROSPHERES, BEAD BLOCK COMPRESSIBLE MICROSPHERES

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510(K) Number: K083091
Device Name: LC BEAD MICROSPHERES, BEAD BLOCK COMPRESSIBLE MICROSPHERES
Manufacturer:
Device Classification Name: Device, Vascular, For Promoting Embolization
Regulation Number: 870.3300
Classification Product Code: KRD
Date Received: 10/17/2008
Decision Date: 12/24/2008
Regulation Medical Specialty: Cardiovascular
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