Modified Amerlex-M Progesterone Radioimmuno. Kit

FDA 510(k) K880934 · Amersham Corp.

Substantially Equivalent

510(k) numberK880934

Submission

Device name
Modified Amerlex-M Progesterone Radioimmuno. Kit
Applicant
Amersham Corp.
Arlington Heights, IL, US
Received
March 7, 1988
Decision date
April 18, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JLS – Radioimmunoassay, Progesterone
Device class
Class I (low risk)
Regulation
21 CFR 862.1620
Specialty
Clinical Chemistry

Other 510(k)s with product code JLS

510(k)DeviceApplicantDecision
K040923Luminescent Immunoassay Kit for the Detection of Progesterone in SalivaJLS · Traditional Ibl GmbH07/22/2004SE
K973898Progesterone ElisaJLS · Traditional Kmi Diagnostics, Inc.11/13/1997SE
K972133Vitros Immunodiagnostics Products Progesterone Reagent Pack (GEM.1070), Progesterone…JLS · Traditional Johnson & Johnson Clinical Diagnostics, Inc.06/24/1997SE
K971725Opus ProgesteroneJLS · Traditional Behring Diagnostics, Inc.06/18/1997SE
K964841Elecsys Progesterone AssayJLS · Traditional Boehringer Mannheim Corp.03/24/1997SE
K965084Vidas Proesterone (PRG) (30 409)JLS · Traditional bioMerieux, Inc.01/09/1997SE
K955025Axsym ProgesteroneJLS · Traditional Abbott Laboratories03/07/1996SE
K955769Access Progesterone AssayJLS · Traditional Bio-Rad Laboratories, Inc.02/05/1996SE
K952075Progesterone Assay for the Technicon Immuno 1 System In-Bitro Diagnostic SystemJLS · Traditional Bayer Corp.06/13/1995SE
K951630Auraflex Progesterone 150TEST PackJLS · Traditional Organon Teknika Corp.05/08/1995SE

More from Organon Teknika Corp.

510(k)DeviceDecision
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K912766Amerlite Ck-Mb AssayJHY · Traditional 07/17/1991SE
K904666Amerlite TSH-60 Assay Product Code: Lan. 0008/2008JLW · Traditional 11/02/1990SE
K902760Amersham TSH Control SeraJJX · Traditional 07/27/1990SE
K901857GADOLINIUM-153 Bone Densitometer (GDC.10413)KGI · Traditional 07/09/1990SE
K901854GADOLINIUM-153 Bone Densitometer (GDC.10411/10412)KGI · Traditional 07/09/1990SE
K901848GADOLINIUM-153 Bone Densitometer SourcesKGI · Traditional 07/09/1990SE
K901832GADOLINIUM-153 Bone Densitometer Sources GDC.10415KGI · Traditional 07/09/1990SE
K896270Amerlite ESTRADIOL-60 Assay LAN.0081/2081CHP · Traditional 12/12/1989SE

Questions and answers

When was Modified Amerlex-M Progesterone Radioimmuno. Kit cleared by the FDA?

Modified Amerlex-M Progesterone Radioimmuno. Kit (K880934) received a 510(k) decision of Substantially Equivalent on April 18, 1988, 42 days after the submission was received.

What is the product code of K880934?

The FDA product code is JLS – Radioimmunoassay, Progesterone, a Class I (low risk) device regulated under 21 CFR 862.1620.