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FDA 510(k), K040512, LIMITED FUNCTION WL/OTC-TENS DEVICE, MODEL WL-2103A, WL-2203A, WL-2203B AND WL-2401
FDA 510(k), K040512, LIMITED FUNCTION WL/OTC-TENS DEVICE, MODEL WL-2103A, WL-2203A, WL-2203B AND WL-2401
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$149.00 USD
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$149.00 USD
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510(K) Number: K040512
Device Name: LIMITED FUNCTION WL/OTC-TENS DEVICE, MODEL WL-2103A, WL-2203A, WL-2203B AND WL-2401
Manufacturer:
Device Classification Name: Stimulator, Nerve, Transcutaneous, For Pain Relief
Regulation Number: 882.5890
Classification Product Code: GZJ
Date Received: 02/27/2004
Decision Date: 05/27/2004
Regulation Medical Specialty: Neurology
Device Name: LIMITED FUNCTION WL/OTC-TENS DEVICE, MODEL WL-2103A, WL-2203A, WL-2203B AND WL-2401
Manufacturer:
Device Classification Name: Stimulator, Nerve, Transcutaneous, For Pain Relief
Regulation Number: 882.5890
Classification Product Code: GZJ
Date Received: 02/27/2004
Decision Date: 05/27/2004
Regulation Medical Specialty: Neurology
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