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

Name: FDA 510(k) clearance K172478
Creator: U.S. Food and Drug Administration
Published: 2018-04-19

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.. Device class: 2.

Clearance details

Applicant: Wat Medical Technology (Ningbo) Co., Ltd.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2017-08-16
Decision date: 2018-04-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ningbo, CN

Download summary PDF View on FDA.gov ↗

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