THYMATRON— 510(k) K843923

Substantially Equivalent

Somatics, Inc.

FDA 510(k) clearance K843923 for THYMATRON, Substantially Equivalent on 1984-12-03. Applicant: Somatics, Inc.. Device class: 2.

Clearance details

Applicant: Somatics, Inc.
Product code: Code QGH
Device class: Class 2
Regulation: 21 CFR 882.5940
Advisory panel: Neurology
Date received: 1984-10-05
Decision date: 1984-12-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Bluff, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code QGH

K192834 — MECTA Sigma2020-04-26
K965070 — SPECTRUM 5000 Q, 5000Q,M,4000 Q, 4000 M.1997-03-06
K960754 — SPECTRUM 5000 Q, 5000 M, 4000 Q, 4000 M1996-09-18
K945120 — THYMATRON 2000 ELECTROCONVULSIVE SYSTEM1995-10-26
K911144 — MF-500, MODIFICATION1991-10-18

More clearances from Somatics, Inc.

K992269 — VENTIL-A ORAL PROTECTOR1999-10-25
K890711 — DUAL GRAPH (TM) RECORDER-MONITOR1989-06-02
K890710 — DISPOSABLE EEG/EKG ELECTRODE, CAT. #EEDS1989-03-14
K882809 — THYMAPAD1988-09-27
K864181 — SOMATICS MOUTH GUARD (BITE BLOCK)1986-11-03

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