MODEL MK II TENS— 510(k) K833251

Name: FDA 510(k) clearance K833251
Creator: U.S. Food and Drug Administration
Published: 1984-03-05

Substantially Equivalent

European Electronic Systems, Ltd.

FDA 510(k) clearance K833251 for MODEL MK II TENS, Substantially Equivalent on 1984-03-05. Applicant: European Electronic Systems, Ltd.. Device class: 2.

Clearance details

Applicant: European Electronic Systems, Ltd.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1983-09-23
Decision date: 1984-03-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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