CENTRIA SYSTEM 2 AUTOMATED METHOD/RIA— 510(k) K801037

Name: FDA 510(k) clearance K801037
Creator: U.S. Food and Drug Administration
Published: 1980-05-28

Substantially Equivalent

Union Carbide Corp.

FDA 510(k) clearance K801037 for CENTRIA SYSTEM 2 AUTOMATED METHOD/RIA, Substantially Equivalent on 1980-05-28. Applicant: Union Carbide Corp.. Device class: 1.

Clearance details

Applicant: Union Carbide Corp.
Product code: Code LCI
Device class: Class 1
Regulation: 21 CFR 862.2050
Advisory panel: Clinical Chemistry
Date received: 1980-05-02
Decision date: 1980-05-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LCI

view all

K983617 — 25-HYDROXYVITAMIN D 125I RIA KIT1998-11-16
K780886 — SYSTEM 6000 AUTOMATED RIA ANALYZER1978-09-01

More clearances from Union Carbide Corp.

view all

K830337 — MARK III OXYGEN WALKER SYS-LOW PRESS1983-03-17
K820836 — MARK III OXYGEN WALKER SYSTEM1982-04-15
K820535 — LASER GAS MIXTURES1982-03-31
K812536 — LINDE MARK II1981-09-23
K810732 — LINDE MARK II OXYGEN RESERV. TYPE OR-41981-03-27

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