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FDA 510(k), K926424, CORTICAL SURF EPILEPSY ELECT DEPTH ELEC EPILEP MON
FDA 510(k), K926424, CORTICAL SURF EPILEPSY ELECT DEPTH ELEC EPILEP MON
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510(K) Number: K926424
Device Name: CORTICAL SURF EPILEPSY ELECT DEPTH ELEC EPILEP MON
Manufacturer: RADIONICS, INC.
Device Classification Name: Electrode, Cortical
Regulation Number: 882.1310
Classification Product Code: GYC
Date Received: 12/23/1992
Decision Date: 11/19/1993
Regulation Medical Specialty: Neurology
Device Name: CORTICAL SURF EPILEPSY ELECT DEPTH ELEC EPILEP MON
Manufacturer: RADIONICS, INC.
Device Classification Name: Electrode, Cortical
Regulation Number: 882.1310
Classification Product Code: GYC
Date Received: 12/23/1992
Decision Date: 11/19/1993
Regulation Medical Specialty: Neurology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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