FDA 510(k), K020020, THE IZZZY-TENS (WL-2401), THE SLIM-TENS (WL-2402), THE MENS-TENS (WL2403), THE COMPACT TENS (WL-2302)

FDA 510(k), K020020, THE IZZZY-TENS (WL-2401), THE SLIM-TENS (WL-2402), THE MENS-TENS (WL2403), THE COMPACT TENS (WL-2302)

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510(K) Number: K020020
Device Name: THE IZZZY-TENS (WL-2401), THE SLIM-TENS (WL-2402), THE MENS-TENS (WL2403), THE COMPACT TENS (WL-2302)
Manufacturer:
Device Classification Name: Stimulator, Nerve, Transcutaneous, For Pain Relief
Regulation Number: 882.5890
Classification Product Code: GZJ
Date Received: 01/03/2002
Decision Date: 12/30/2002
Regulation Medical Specialty: Neurology
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