Dac-Cel T4

FDA 510(k) K791231 · Burroughs Wellcome Co.

Substantially Equivalent

510(k) numberK791231

Submission

Device name
Dac-Cel T4
Applicant
Burroughs Wellcome Co.
Mchenry, IL, US
Received
July 2, 1979
Decision date
September 4, 1979
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
K820069Wellcogen Group BGTZ · Traditional 02/18/1982SE
K813508Sac-CelKTS · Traditional 12/29/1981SE
K810215Dac-Cel HCGJHI · Traditional 04/17/1981SE
K810214Dac-Cel DiagnatalJHI · Traditional 03/06/1981SE
K810213Dac-Cel TSHJLW · Traditional 02/10/1981SE
K810212Dac-Cel T3 UptakeKHQ · Traditional 02/10/1981SE
K791232Dac-Cel T3CDP · Traditional 09/04/1979SE
K781607Strep-TexGTZ · Traditional 10/17/1978SE
K780874Thymune-TDDC · Traditional 06/14/1978SE
K780873Thymune-MDDC · Traditional 06/14/1978SE

Questions and answers

When was Dac-Cel T4 cleared by the FDA?

Dac-Cel T4 (K791231) received a 510(k) decision of Substantially Equivalent on September 4, 1979, 64 days after the submission was received.

What is the product code of K791231?

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