FDA 510(k), K181955, WiEMSpro

FDA 510(k), K181955, WiEMSpro

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510(K) Number: K181955
Device Name: WiEMSpro
Manufacturer: Medical Cables, S.L.
Device Classification Name: stimulator, muscle, powered, for muscle conditioning
Regulation Number: 890.5850
Classification Product Code: NGX
Date Received: 07/23/2018
Decision Date: 02/12/2019
Regulation Medical Specialty: Physical Medicine

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