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FDA 510(k), K042231, GELSPHERES MICROSPHERES AND BEAD BLOCK COMPRESSIBLE MICROSPHERES
FDA 510(k), K042231, GELSPHERES MICROSPHERES AND BEAD BLOCK COMPRESSIBLE MICROSPHERES
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$149.00 USD
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510(K) Number: K042231
Device Name: GELSPHERES MICROSPHERES AND BEAD BLOCK COMPRESSIBLE MICROSPHERES
Manufacturer:
Device Classification Name: Device, Neurovascular Embolization
Regulation Number: 882.5950
Classification Product Code: HCG
Date Received: 08/17/2004
Decision Date: 11/12/2004
Regulation Medical Specialty: Neurology
Device Name: GELSPHERES MICROSPHERES AND BEAD BLOCK COMPRESSIBLE MICROSPHERES
Manufacturer:
Device Classification Name: Device, Neurovascular Embolization
Regulation Number: 882.5950
Classification Product Code: HCG
Date Received: 08/17/2004
Decision Date: 11/12/2004
Regulation Medical Specialty: Neurology
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