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FDA 510(k), K921319, NEUROMED MODEL OCA-30 OCTODE AND MODEL SCA-30
FDA 510(k), K921319, NEUROMED MODEL OCA-30 OCTODE AND MODEL SCA-30
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510(K) Number: K921319
Device Name: NEUROMED MODEL OCA-30 OCTODE AND MODEL SCA-30
Manufacturer: NEUROMED, INC.
Device Classification Name: stimulator, spinal-cord, implanted (pain relief)
Regulation Number: 882.5880
Classification Product Code: GZB
Date Received: 03/19/1992
Decision Date: 05/05/1993
Regulation Medical Specialty: Neurology
Device Name: NEUROMED MODEL OCA-30 OCTODE AND MODEL SCA-30
Manufacturer: NEUROMED, INC.
Device Classification Name: stimulator, spinal-cord, implanted (pain relief)
Regulation Number: 882.5880
Classification Product Code: GZB
Date Received: 03/19/1992
Decision Date: 05/05/1993
Regulation Medical Specialty: Neurology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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