Ria Kit, T4 Clasp

FDA 510(k) K770726 · Squibb & Sons, Inc.

Substantially Equivalent

510(k) numberK770726

Submission

Device name
Ria Kit, T4 Clasp
Applicant
Squibb & Sons, Inc.
Mchenry, IL, US
Received
April 19, 1977
Decision date
April 28, 1977
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
K821174Tsh-Squibb Radioimmunoassay KitJLW · Traditional 05/14/1982SE
K801424Estriol Ria Kit for Use with GammafloCGI · Traditional 07/21/1980SE
K800750Stomahesive Sterile WaferEXB · Traditional 05/08/1980SE
K761267Angiotensin I Immutope KitCIB · Traditional 12/30/1976SE

Questions and answers

When was Ria Kit, T4 Clasp cleared by the FDA?

Ria Kit, T4 Clasp (K770726) received a 510(k) decision of Substantially Equivalent on April 28, 1977, 9 days after the submission was received.

What is the product code of K770726?

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