T3 UPTAKE KIT— 510(k) K810857

Substantially Equivalent

Immuno Assay Corp.

FDA 510(k) clearance K810857 for T3 UPTAKE KIT, Substantially Equivalent on 1981-04-08. Applicant: Immuno Assay Corp.. Device class: 2.

Clearance details

Applicant: Immuno Assay Corp.
Product code: Code KHQ
Device class: Class 2
Regulation: 21 CFR 862.1715
Advisory panel: Clinical Chemistry
Date received: 1981-03-30
Decision date: 1981-04-08
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 Immuno Assay Corp.

K833842 — RIA COAT DIGOXIN1984-01-17
K833745 — RIACOAT T-41984-01-04
K820074 — CORTISOL (RIA) KIT1982-01-28
K820089 — TSH (RIA) KIT1982-01-28
K811954 — COMBO-FER IRON DIAGNOSTIC1981-07-27

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