T3 UPTAKE KITS— 510(k) K822612

Substantially Equivalent

Pcl-Ria, Inc.

FDA 510(k) clearance K822612 for T3 UPTAKE KITS, Substantially Equivalent on 1982-09-30. Applicant: Pcl-Ria, Inc.. Device class: 2.

Clearance details

Applicant: Pcl-Ria, Inc.
Product code: Code KHQ
Device class: Class 2
Regulation: 21 CFR 862.1715
Advisory panel: Clinical Chemistry
Date received: 1982-08-30
Decision date: 1982-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KHQ

K981375 — ACE T UPTAKE REAGENT TU CALIBRATORS1998-06-10
K980088 — T-UPTAKE MICROPLATE EIA1998-02-04
K970539 — CHIRON DIAGNOSTICS ACS:180TU P1997-03-24
K964308 — VITROS IMMUNODIAGNOSTICS PRODUCTS T3 UPTAKE REAGENT PACK (GEM.1025) AND T3 UPTAKE CALIBRATORS (GEM.C025)1996-11-27
K961488 — ELECSYS T-UPTAKE ASSAY1996-06-12

More clearances from Pcl-Ria, Inc.

K830526 — B-GCG SYSTEM BY RIA1983-04-05
K822935 — THYROID STIMULATING HORMONE1982-11-01
K823014 — DIGOXIN KIT1982-11-01
K820886 — THYROXINE T4 KIT1982-04-16
K820358 — FOLLICLE STIMULATING HORMONE KIT1982-03-26

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