AUTO-TENS MODEL III DUAL CHANNEL REPLACE— 510(k) K823466

Name: FDA 510(k) clearance K823466
Creator: U.S. Food and Drug Administration
Published: 1983-03-07

Substantially Equivalent

Cbc Corp.

FDA 510(k) clearance K823466 for AUTO-TENS MODEL III DUAL CHANNEL REPLACE, Substantially Equivalent on 1983-03-07. Applicant: Cbc Corp.. Device class: 2.

Clearance details

Applicant: Cbc Corp.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1982-11-19
Decision date: 1983-03-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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