IMMUBEAD THYROID UPTAKE— 510(k) K872172

Substantially Equivalent

Immunotech Corp.

FDA 510(k) clearance K872172 for IMMUBEAD THYROID UPTAKE, Substantially Equivalent on 1987-08-17. Applicant: Immunotech Corp.. Device class: 2.

Clearance details

Applicant: Immunotech Corp.
Product code: Code KHQ
Device class: Class 2
Regulation: 21 CFR 862.1715
Advisory panel: Clinical Chemistry
Date received: 1987-06-08
Decision date: 1987-08-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boston, MA, 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 Immunotech Corp.

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K952789 — OPTICLONE CD4FITC/CD8 PE MONOCLONAL ANTIBODIES1995-08-14
K950626 — OPTICLONE CD3/CD4 MONOCLONAL ANTIBODIES1995-05-05
K931228 — PROGESTERONE RADIOIMMUNOASSAY KIT1993-10-22
K911634 — MICROZYME(TM) FREE T4 ENZYME IMMUNOASSAY TEST1991-06-24

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