AUTO-TENS MODEL V— 510(k) K832337

Substantially Equivalent

Cbc Corp.

FDA 510(k) clearance K832337 for AUTO-TENS MODEL V, Substantially Equivalent on 1983-08-31. 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: 1983-07-18
Decision date: 1983-08-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Cbc Corp.

K823466 — AUTO-TENS MODEL III DUAL CHANNEL REPLACE1983-03-07
K823467 — AUTO-TENS MODEL I DISPOS. SINGLE CHAN1983-02-07
K823464 — AUTO-TENS MODEL IV -DUAL CHANNEL FULL1983-02-02
K823465 — AUTO-TENS MODEL II SINGLE CHANNEL1983-02-02

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