HAND HELD GONIOMETER— 510(k) K850082

Substantially Equivalent

Chattanooga Group, Inc.

FDA 510(k) clearance K850082 for HAND HELD GONIOMETER, Substantially Equivalent on 1985-04-04. Applicant: Chattanooga Group, Inc.. Device class: 1.

Clearance details

Applicant: Chattanooga Group, Inc.
Product code: Code KQW
Device class: Class 1
Regulation: 21 CFR 888.1520
Advisory panel: Orthopedic
Date received: 1985-01-10
Decision date: 1985-04-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Red Bank, TN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KQW

K926237 — O'BRIEN GONIOMETER1993-08-02
K901744 — DOBBHOFF(R) RETRIEVAL FORCEPS1990-07-03
K870767 — THE (CROM) TESTER1987-03-17
K831550 — FINGER BONIOMETER BK75061983-06-24
K812778 — THE TELOS EQUIPMENT1981-12-08

More clearances from Chattanooga Group, Inc.

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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.