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FDA 510(k), K131251, TRINITY ELE
FDA 510(k), K131251, TRINITY ELE
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510(K) Number: K131251
Device Name: TRINITY ELE
Manufacturer: Carol Cole Company
Device Classification Name: stimulator, transcutaneous electrical, aesthetic purposes
Regulation Number: 882.5890
Classification Product Code: NFO
Date Received: 05/01/2013
Decision Date: 10/01/2013
Regulation Medical Specialty: Neurology
Device Name: TRINITY ELE
Manufacturer: Carol Cole Company
Device Classification Name: stimulator, transcutaneous electrical, aesthetic purposes
Regulation Number: 882.5890
Classification Product Code: NFO
Date Received: 05/01/2013
Decision Date: 10/01/2013
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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