FDA 510(k), K132660, NERVE CUFF
FDA 510(k), K132660, NERVE CUFF
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510(K) Number: K132660
Device Name: NERVE CUFF
Manufacturer:
Device Classification Name: Cuff, Nerve
Regulation Number: 882.5275
Classification Product Code: JXI
Date Received: 08/26/2013
Decision Date: 01/10/2014
Regulation Medical Specialty: Neurology
Device Name: NERVE CUFF
Manufacturer:
Device Classification Name: Cuff, Nerve
Regulation Number: 882.5275
Classification Product Code: JXI
Date Received: 08/26/2013
Decision Date: 01/10/2014
Regulation Medical Specialty: Neurology