TENS DEVICE— 510(k) K812138

Substantially Equivalent

Western Advanced Technology, Inc.

FDA 510(k) clearance K812138 for TENS DEVICE, Substantially Equivalent on 1981-08-20. Applicant: Western Advanced Technology, Inc.. Device class: 2.

Clearance details

Applicant: Western Advanced Technology, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1981-07-28
Decision date: 1981-08-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K811790 — OCTOTOXIC SCREENER1981-07-15
K802324 — E1 SERIES HEARING AID1980-10-10

Data sourced from openFDA. This site is unofficial and independent of the FDA.