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FDA 510(k), K081943, MODEL ES-130
FDA 510(k), K081943, MODEL ES-130
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510(K) Number: K081943
Device Name: MODEL ES-130
Manufacturer: KENNETH L BLOCK
Device Classification Name: Stimulator, Electro-Acupuncture
Regulation Number: BWK
Classification Product Code: 07/08/2008
Date Received: 11/24/2008
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
Device Name: MODEL ES-130
Manufacturer: KENNETH L BLOCK
Device Classification Name: Stimulator, Electro-Acupuncture
Regulation Number: BWK
Classification Product Code: 07/08/2008
Date Received: 11/24/2008
Decision Date: Substantially Equivalent (SESE)
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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