FDA 510(k), K100441, XINIWAVE, MODEL XW-18

FDA 510(k), K100441, XINIWAVE, MODEL XW-18

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510(K) Number: K100441
Device Name: XINIWAVE, MODEL XW-18
Manufacturer:
Device Classification Name: Stimulator, Nerve, Transcutaneous, Over-The-Counter
Regulation Number: 882.5890
Classification Product Code: NUH
Date Received: 02/17/2010
Decision Date: 07/15/2010
Regulation Medical Specialty: Neurology
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