FDA 510(k), K094018, LC BEAD MICROSPHERES, BEAD BLOCK COMPRESSIBLE MICROSPHERES
FDA 510(k), K094018, LC BEAD MICROSPHERES, BEAD BLOCK COMPRESSIBLE MICROSPHERES
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510(K) Number: K094018
Device Name: LC BEAD MICROSPHERES, BEAD BLOCK COMPRESSIBLE MICROSPHERES
Manufacturer:
Device Classification Name: Device, Neurovascular Embolization
Regulation Number: 882.5950
Classification Product Code: HCG
Date Received: 12/29/2009
Decision Date: 04/16/2010
Regulation Medical Specialty: Neurology
Device Name: LC BEAD MICROSPHERES, BEAD BLOCK COMPRESSIBLE MICROSPHERES
Manufacturer:
Device Classification Name: Device, Neurovascular Embolization
Regulation Number: 882.5950
Classification Product Code: HCG
Date Received: 12/29/2009
Decision Date: 04/16/2010
Regulation Medical Specialty: Neurology