T-3 UPTAKE/RIASSAY— 510(k) K855033

Substantially Equivalent

Ria Diagnostics

FDA 510(k) clearance K855033 for T-3 UPTAKE/RIASSAY, Substantially Equivalent on 1986-01-24. Applicant: Ria Diagnostics. Device class: 2.

Clearance details

Applicant: Ria Diagnostics
Product code: Code KHQ
Device class: Class 2
Regulation: 21 CFR 862.1715
Advisory panel: Clinical Chemistry
Date received: 1985-12-17
Decision date: 1986-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Fe Springs, CA, 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 Ria Diagnostics

K854798 — T-4 RIASSAY1986-01-15
K852537 — T-3 RIASSAY1985-08-12
K810296 — DIGOXIN RIA ASSAY1981-02-19
K801691 — TSH RIASSAY1980-08-27
K792062 — THEOPHYLLINE RIASSAY1980-02-25

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