FDA 510(k), K032115, NEUROLAC NERVE GUIDE MODELS NG01-15/03, NG01-020/03, NG01 025/03, NG01-030/03
FDA 510(k), K032115, NEUROLAC NERVE GUIDE MODELS NG01-15/03, NG01-020/03, NG01 025/03, NG01-030/03
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$149.00 USD
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510(K) Number: K032115
Device Name: NEUROLAC NERVE GUIDE MODELS NG01-15/03, NG01-020/03, NG01 025/03, NG01-030/03
Manufacturer:
Device Classification Name: Cuff, Nerve
Regulation Number: 882.5275
Classification Product Code: JXI
Date Received: 07/09/2003
Decision Date: 10/10/2003
Regulation Medical Specialty: Neurology
Device Name: NEUROLAC NERVE GUIDE MODELS NG01-15/03, NG01-020/03, NG01 025/03, NG01-030/03
Manufacturer:
Device Classification Name: Cuff, Nerve
Regulation Number: 882.5275
Classification Product Code: JXI
Date Received: 07/09/2003
Decision Date: 10/10/2003
Regulation Medical Specialty: Neurology