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FDA 510(k), K090042, PAINMASTER MCT PATCH
FDA 510(k), K090042, PAINMASTER MCT PATCH
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510(K) Number: K090042
Device Name: PAINMASTER MCT PATCH
Manufacturer: NEWMARK, INC.
Device Classification Name: stimulator, nerve, transcutaneous, over-the-counter
Regulation Number: 882.5890
Classification Product Code: NUH
Date Received: 01/06/2009
Decision Date: 05/06/2009
Regulation Medical Specialty: Neurology
Device Name: PAINMASTER MCT PATCH
Manufacturer: NEWMARK, INC.
Device Classification Name: stimulator, nerve, transcutaneous, over-the-counter
Regulation Number: 882.5890
Classification Product Code: NUH
Date Received: 01/06/2009
Decision Date: 05/06/2009
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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