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FDA 510(k), K961749, TRANSAMERICA ELECTRODE
FDA 510(k), K961749, TRANSAMERICA ELECTRODE
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510(K) Number: K961749
Device Name: TRANSAMERICA ELECTRODE
Manufacturer: TRANSAMERICA MEDICAL SYSTEMS
Device Classification Name: stimulator, nerve, transcutaneous, for pain relief
Regulation Number: 882.5890
Classification Product Code: GZJ
Date Received: 03/25/1996
Decision Date: 06/21/1996
Regulation Medical Specialty: Neurology
Device Name: TRANSAMERICA ELECTRODE
Manufacturer: TRANSAMERICA MEDICAL SYSTEMS
Device Classification Name: stimulator, nerve, transcutaneous, for pain relief
Regulation Number: 882.5890
Classification Product Code: GZJ
Date Received: 03/25/1996
Decision Date: 06/21/1996
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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