TYTRON C-3000— 510(k) K974208

Name: FDA 510(k) clearance K974208
Creator: U.S. Food and Drug Administration
Published: 1998-02-03

Substantially Equivalent

Titronics Research & Development Co.

FDA 510(k) clearance K974208 for TYTRON C-3000, Substantially Equivalent on 1998-02-03. Applicant: Titronics Research & Development Co.. Device class: 2.

Clearance details

Applicant: Titronics Research & Development Co.
Product code: Code HCS
Device class: Class 2
Regulation: 21 CFR 882.1570
Advisory panel: Neurology
Date received: 1997-11-10
Decision date: 1998-02-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oxford, IA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HCS

view all

K981805 — POS T-70001998-08-07
K950986 — NEUROREADER1995-11-09
K894772 — THERMALGRAPHIC ANALYSER1989-10-03
K840487 — T-METER1984-03-12
K831995 — TRENDO-SCOPE1983-08-08

More clearances from Titronics Research & Development Co.

view all

K032471 — TYTRON C-500IR CLINICAL INFRARED IMAGING SYSTEM2003-10-10

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