TENS device-EmeTerm 2, Model: YF-ZTY-E2— 510(k) K220503

Name: FDA 510(k) clearance K220503
Creator: U.S. Food and Drug Administration
Published: 2022-04-23

Substantially Equivalent

Wat Medical Technology, Inc.

FDA 510(k) clearance K220503 for TENS device-EmeTerm 2, Model: YF-ZTY-E2, Substantially Equivalent on 2022-04-23. Applicant: Wat Medical Technology, Inc.. Device class: 2.

Clearance details

Applicant: Wat Medical Technology, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2022-02-22
Decision date: 2022-04-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ningbo, CN

Download summary PDF View on FDA.gov ↗

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