CBR-T3 UPTAKE KIT— 510(k) K780500

Substantially Equivalent

Clinical Bioresearch

FDA 510(k) clearance K780500 for CBR-T3 UPTAKE KIT, Substantially Equivalent on 1978-05-03. Applicant: Clinical Bioresearch. Device class: 2.

Clearance details

Applicant: Clinical Bioresearch
Product code: Code KHQ
Device class: Class 2
Regulation: 21 CFR 862.1715
Advisory panel: Clinical Chemistry
Date received: 1978-03-28
Decision date: 1978-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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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 Clinical Bioresearch

K780707 — T4-RIA KIT1978-06-14
K780499 — CBR-T3RIA KIT1978-05-04
K780498 — CBR-DIGOXIN ANTISERUM1978-04-05

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