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FDA 510(k), K852920, QUADRA CATH ELECT(3MM SIZES) 1990J, JF, JP + JPF
FDA 510(k), K852920, QUADRA CATH ELECT(3MM SIZES) 1990J, JF, JP + JPF
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510(K) Number: K852920
Device Name: QUADRA CATH ELECT(3MM SIZES) 1990J, JF, JP + JPF
Manufacturer: NEUROMED, INC.
Device Classification Name: stimulator, spinal-cord, implanted (pain relief)
Regulation Number: 882.5880
Classification Product Code: GZB
Date Received: 07/10/1985
Decision Date: 10/10/1985
Regulation Medical Specialty: Neurology
Device Name: QUADRA CATH ELECT(3MM SIZES) 1990J, JF, JP + JPF
Manufacturer: NEUROMED, INC.
Device Classification Name: stimulator, spinal-cord, implanted (pain relief)
Regulation Number: 882.5880
Classification Product Code: GZB
Date Received: 07/10/1985
Decision Date: 10/10/1985
Regulation Medical Specialty: Neurology
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