Ciba Corning Magic Lite Chlamydia Immunoassay

FDA 510(k) K895122 · Ciba Corning Diagnostics Corp.

Substantially Equivalent

510(k) numberK895122

Submission

Device name
Ciba Corning Magic Lite Chlamydia Immunoassay
Applicant
Ciba Corning Diagnostics Corp.
East Walpole, MA, US
Received
August 15, 1989
Decision date
October 30, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LJC – Enzyme Linked Immunoabsorbent Assay, (Chlamydiae Group)
Device class
Class I (low risk)
Regulation
21 CFR 866.3120
Specialty
Microbiology

Other 510(k)s with product code LJC

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K032330CT OiaLJC · Traditional Thermo Biostar, Inc.03/02/2004SE
K033865Ideia Pce ChlamydiaLJC · Special Dakocytomation, Ltd.01/21/2004SE
K033079Chlamydia Igg Elisa Test SystemLJC · Traditional Trinity Biotech USA11/26/2003SE
K982210Modification of Syva Microtrak II Chlamydia EiaLJC · Special Dade Behring, Inc.07/09/1998SE
K962558Chlamydia Igg Elisa Test SystemLJC · Traditional Armkel, LLC02/24/1997SE
K960850Access Chlamydia AssayLJC · Traditional Bio-Rad Laboratories, Inc.02/04/1997SE
K955627Vidas Chlamydia Blocking AssayLJC · Traditional Biomerieux Vitek, Inc.10/07/1996SE
K936054Imx Select ChlamydiaLJC · Traditional Abbott Laboratories05/30/1996SE
K940564Ideia(Tm) Chlamydia Blocking Reagents, ModificationLJC · Traditional Dako Diagnostics , Ltd.01/11/1996SE
K951010Chlamydia OiaLJC · Traditional Biostar, Inc.10/07/1995SE

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Questions and answers

When was Ciba Corning Magic Lite Chlamydia Immunoassay cleared by the FDA?

Ciba Corning Magic Lite Chlamydia Immunoassay (K895122) received a 510(k) decision of Substantially Equivalent on October 30, 1989, 76 days after the submission was received.

What is the product code of K895122?

The FDA product code is LJC – Enzyme Linked Immunoabsorbent Assay, (Chlamydiae Group), a Class I (low risk) device regulated under 21 CFR 866.3120.