INTELECT 210 PORTABLE ULTRASOUND— 510(k) K841447

Name: FDA 510(k) clearance K841447
Creator: U.S. Food and Drug Administration
Published: 1984-05-09

Substantially Equivalent

Chattanooga Group, Inc.

FDA 510(k) clearance K841447 for INTELECT 210 PORTABLE ULTRASOUND, Substantially Equivalent on 1984-05-09. Applicant: Chattanooga Group, Inc.. Device class: 2.

Clearance details

Applicant: Chattanooga Group, Inc.
Product code: Code IMI
Device class: Class 2
Regulation: 21 CFR 890.5300
Advisory panel: Physical Medicine
Date received: 1984-04-06
Decision date: 1984-05-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IMI

view all

K240788 — Ultrasound Stimulator2025-06-04
K230472 — Sonopuls 1902023-10-24
K222098 — ManaSport+2023-03-08
K210284 — ManaSport2022-04-26
K202788 — Sonomed IV, Sonomed V2021-12-23

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.