Cidba Corning Acs Cortisol Immunoassay

FDA 510(k) K934317 · Ciba Corning Diagnostics Corp.

Substantially Equivalent

510(k) numberK934317

Submission

Device name
Cidba Corning Acs Cortisol Immunoassay
Applicant
Ciba Corning Diagnostics Corp.
Medfield, MA, US
Received
September 1, 1993
Decision date
May 13, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JFT – Fluorometric, Cortisol
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1205
Specialty
Clinical Chemistry

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K062204Architect Cortisol AssayJFT · Traditional Seradyn, Inc.09/22/2006SE
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K021218Elecsys Cortisol Test SystemJFT · Traditional Roche Diagnostics Corp.09/09/2002SE
K962559Acs Cortisol ImmunoassayJFT · Traditional Ciba Corning Diagnostics Corp.11/05/1996SE
K954591Aia-Pack Cort AssayJFT · Traditional Tosoh Medics, Inc.12/15/1995SE
K931031Vidas Cortisol (Cort) Assay & Serum Free DilutentJFT · Traditional Biomerieux Vitek, Inc.07/27/1993SE

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K962021Ciba Corning 348 SystemCHL · Traditional 06/24/1996SE
K962126Acs CKMB II ImmunoassayJHS · Traditional 06/21/1996SE
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K961510Acs FRT4 ImmunoassayJJX · Traditional 06/17/1996SE
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Questions and answers

When was Cidba Corning Acs Cortisol Immunoassay cleared by the FDA?

Cidba Corning Acs Cortisol Immunoassay (K934317) received a 510(k) decision of Substantially Equivalent on May 13, 1994, 254 days after the submission was received.

What is the product code of K934317?

The FDA product code is JFT – Fluorometric, Cortisol, a Class II (moderate risk) device regulated under 21 CFR 862.1205.