TENS device-EmeTerm, CinvStop— 510(k) K172478

Substantially Equivalent

Wat Medical Technology (Ningbo) Co., Ltd.

FDA 510(k) clearance K172478 for TENS device-EmeTerm, CinvStop, Substantially Equivalent on 2018-04-19. Applicant: Wat Medical Technology (Ningbo) Co., Ltd..

Clearance details

Applicant: Wat Medical Technology (Ningbo) Co., Ltd.
Product code: Code GZJ
Advisory panel: Neurology
Date received: 2017-08-16
Decision date: 2018-04-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ningbo, CN

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