Delfia Thyroxine (T4) Kit

FDA 510(k) K883559 · Pharmacia, Inc.

Substantially Equivalent

510(k) numberK883559

Submission

Device name
Delfia Thyroxine (T4) Kit
Applicant
Pharmacia, Inc.
Piscataway, NJ, US
Received
August 19, 1988
Decision date
December 14, 1988
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

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K970420Mastercap Am 5.0/MASTERCAP RM 5.0JQW · Traditional 06/30/1997SE
K964152Unicap Total Ige Assay/Pharmacia Total Ige Controls LMHDGC · Traditional 04/23/1997SE
K962274Unicap 100DHB · Traditional 09/12/1996SE
K941993Pharmacia Cap System Phadiatop FeiaDHB · Traditional 01/30/1996SE
K954337Genotropin MixerFMF · Traditional 11/13/1995SE
K951025Piston SyringeFMF · Traditional 10/19/1995SE
K952025RobocapJQW · Traditional 07/26/1995SE

Questions and answers

When was Delfia Thyroxine (T4) Kit cleared by the FDA?

Delfia Thyroxine (T4) Kit (K883559) received a 510(k) decision of Substantially Equivalent on December 14, 1988, 117 days after the submission was received.

What is the product code of K883559?

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