MEDIUM FREQU. ELEC. MUSCLE STIMULATOR— 510(k) K850698

Name: FDA 510(k) clearance K850698
Creator: U.S. Food and Drug Administration
Published: 1985-05-17

Substantially Equivalent

Chattanooga Group, Inc.

FDA 510(k) clearance K850698 for MEDIUM FREQU. ELEC. MUSCLE STIMULATOR, Substantially Equivalent on 1985-05-17. Applicant: Chattanooga Group, Inc.. Device class: 2.

Clearance details

Applicant: Chattanooga Group, Inc.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1985-02-21
Decision date: 1985-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Red Bank, TN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IPF

view all

K253542 — Apollo Quattro (APQ-10M)2026-06-08
K252816 — High Tone Power therapy (HiToP) (Model: HiToP PNP)2026-06-02
K260142 — StimelMD (SSMD) system2026-05-27
K251083 — Compact II2025-09-12
K241433 — EVE Synergy (EVE-20M)2025-06-04

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.