Thyroxine Stds. in Human Serum

FDA 510(k) K780050 · Pcl-Ria, Inc.

Substantially Equivalent

510(k) numberK780050

Submission

Device name
Thyroxine Stds. in Human Serum
Applicant
Pcl-Ria, Inc.
Mchenry, IL, US
Received
January 9, 1978
Decision date
February 13, 1978
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CDX – Radioimmunoassay, Total Thyroxine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1700
Specialty
Clinical Chemistry

Other 510(k)s with product code CDX

510(k)DeviceApplicantDecision
K961490Elecsys T4 AssayCDX · Traditional Boehringer Mannheim Corp.06/13/1996SE
K954312Active Thyroxine RiaCDX · Traditional Diagnostic Systems Laboratories, Inc.10/07/1995SE
K943416Delfia Neonatal Thyroxine KitCDX · Traditional Wallac OY03/10/1995SE
K934384Axsym(Tm) Total T4CDX · Traditional Abbott Laboratories06/21/1994SE
K932980Total T4 Fpia Reagent Set/Calibrator #T-1039,T-116CDX · Traditional Sigma Diagnostics, Inc.10/18/1993SE
K933426Stratus(R) Total THYROXINE(T4) Fluor Enzyme ImmunoCDX · Traditional Baxter Diagnostics, Inc.08/26/1993SE
K931295Iq TT4 AssayCDX · Traditional Becton Dickinson Advanced Diagnostics07/20/1993SE
K926563Autobead(Tm) T4 Enzyme Immunoassay Test KitCDX · Traditional Bio-Chem Laboratory Systems, Inc.03/18/1993SE
K925110Abbott Imx T4CDX · Traditional Abbott Laboratories01/26/1993SE
K925109Abbott Tdx/Tdxflx TT4CDX · Traditional Abbott Laboratories01/04/1993SE

More from Abbott Laboratories

510(k)DeviceDecision
K830526B-Gcg System by RiaJHI · Traditional 04/05/1983SE
K823014Digoxin KitDPB · Traditional 11/01/1982SE
K822935Thyroid Stimulating HormoneJLW · Traditional 11/01/1982SE
K822612T3 Uptake KitsKHQ · Traditional 09/30/1982SE
K820886Thyroxine T4 KitCDX · Traditional 04/16/1982SE
K820358Follicle Stimulating Hormone KitCGJ · Traditional 03/26/1982SE
K820357Luteinizing Hormone KitCEP · Traditional 03/25/1982SE
K812666Thyroxine (T4) 125ICDP · Traditional 10/02/1981SE
K810867Follicle Stimulating Hormone (FSH)JIS · Traditional 04/14/1981SE
K810852Follicle Stimulating Hormone AntiserumCGJ · Traditional 04/08/1981SE

Questions and answers

When was Thyroxine Stds. in Human Serum cleared by the FDA?

Thyroxine Stds. in Human Serum (K780050) received a 510(k) decision of Substantially Equivalent on February 13, 1978, 35 days after the submission was received.

What is the product code of K780050?

The FDA product code is CDX – Radioimmunoassay, Total Thyroxine, a Class II (moderate risk) device regulated under 21 CFR 862.1700.