KC/EMG DIAGNOSTIC ELECTROMYOGRAPH— 510(k) K864630

Name: FDA 510(k) clearance K864630
Creator: U.S. Food and Drug Administration
Published: 1986-12-29

Substantially Equivalent

Chattanooga Group, Inc.

FDA 510(k) clearance K864630 for KC/EMG DIAGNOSTIC ELECTROMYOGRAPH, Substantially Equivalent on 1986-12-29. Applicant: Chattanooga Group, Inc.. Device class: 2.

Clearance details

Applicant: Chattanooga Group, Inc.
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 1986-11-25
Decision date: 1986-12-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Red Bank, TN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IKN

view all

K172743 — Natus VikingQuest2017-12-19
K163150 — ViMove22017-07-14
K162383 — Cadwell Sierra Summit, Cadwell Sierra Ascent2017-03-01
K142494 — ViMove2015-05-28
K131094 — VIMOVE2014-07-11

More clearances from Chattanooga Group, Inc.

view all

K011243 — CHATTANOOGA DRY HEAT WHIRLPOOL, MODEL 20002001-07-06
K982317 — VECTRA COMBO1999-02-01
K982321 — VECTRA STIM MODELS 200 AND 4001999-02-01
K982324 — VECTRA PRO MODELS 2 AND 41999-02-01
K982828 — FORTE, MODELS CPS 400 STIM, CPS 200 STIM1998-11-06

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