FDA 510(k), K930536, NEUROMED OCTRODE MODEL MNR-88A-B-C NEUROSTIM REC

FDA 510(k), K930536, NEUROMED OCTRODE MODEL MNR-88A-B-C NEUROSTIM REC

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510(K) Number: K930536
Device Name: NEUROMED OCTRODE MODEL MNR-88A-B-C NEUROSTIM REC
Manufacturer: NEUROMED, INC.
Device Classification Name: stimulator, spinal-cord, implanted (pain relief)
Regulation Number: 882.5880
Classification Product Code: GZB
Date Received: 01/27/1993
Decision Date: 12/15/1994
Regulation Medical Specialty: Neurology

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