Ciba Corning Acs Progesterone Immunoassay

FDA 510(k) K932955 · Ciba Corning Diagnostics Corp.

Substantially Equivalent

510(k) numberK932955

Submission

Device name
Ciba Corning Acs Progesterone Immunoassay
Applicant
Ciba Corning Diagnostics Corp.
East Walpole, MA, US
Received
June 17, 1993
Decision date
August 2, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

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

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Questions and answers

When was Ciba Corning Acs Progesterone Immunoassay cleared by the FDA?

Ciba Corning Acs Progesterone Immunoassay (K932955) received a 510(k) decision of Substantially Equivalent on August 2, 1993, 46 days after the submission was received.

What is the product code of K932955?

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