FDA 510(k), K011702, VERTIS PNT CONTROL UNIT, VERTIS PNT SAFEGUIDE KIDS, MODELS CU100, SGXXX

FDA 510(k), K011702, VERTIS PNT CONTROL UNIT, VERTIS PNT SAFEGUIDE KIDS, MODELS CU100, SGXXX

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510(K) Number: K011702
Device Name: VERTIS PNT CONTROL UNIT, VERTIS PNT SAFEGUIDE KIDS, MODELS CU100, SGXXX
Manufacturer:
Device Classification Name: Stimulator, Nerve, Electrical, Percutaneous (Pens), For Pain Relief
Regulation Number: 882.5890
Classification Product Code: NHI
Date Received: 06/01/2001
Decision Date: 12/21/2001
Regulation Medical Specialty: Neurology
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