Acs: 180 and Advia Centaur Theophylline 2 Assay

FDA 510(k) K013272 · Bayer Corp.

Substantially Equivalent

510(k) numberK013272

Submission

Device name
Acs: 180 and Advia Centaur Theophylline 2 Assay
Applicant
Bayer Corp.
Tarrytown, NY, US
Received
October 1, 2001
Decision date
October 25, 2001
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KLS – Enzyme Immunoassay, Theophylline
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3880
Specialty
Clinical Toxicology

Other 510(k)s with product code KLS

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K042520Vitros Chemistry Products Caffn Reagent Kit and TDM Performance Verifiers I, II and IIIKLS · Traditional Ortho-Clinical Diagnostics, Inc.11/30/2004SE
K042407Emit Caffeine AssayKLS · Traditional Dade Behring, Inc.10/28/2004SE
K020740Roche Online TheophyllineKLS · Traditional Roche Diagnostics Corp.04/16/2002SE
K011771Randox TheophyllineKLS · Traditional Randox Laboratories, Ltd.01/17/2002SE
K011166Modification to Emit 2000 Theophylline Assay, Model Osr 4P229KLS · Special Syva Co., Dade Behring, Inc.05/10/2001SE
K993029Abbott Aeroset Theophylline Assay and Calibrators; Models 1E09 and 6E89KLS · Traditional Syva Co.01/27/2000SE
K973583Ace Theophylline Reagent, Theo CalibratorsKLS · Traditional Schiapparelli Biosystems, Inc.11/12/1997SE
K972495Accumeter Theophylline TestKLS · Traditional Chemtrak, Inc.10/10/1997SE
K961462Cedia Theophylline AssayKLS · Traditional Boehringer Mannheim Corp.06/27/1996SE
K954569Immulite TheophyllineKLS · Traditional Diagnostic Products Corp.11/13/1995SE

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Questions and answers

When was Acs: 180 and Advia Centaur Theophylline 2 Assay cleared by the FDA?

Acs: 180 and Advia Centaur Theophylline 2 Assay (K013272) received a 510(k) decision of Substantially Equivalent on October 25, 2001, 24 days after the submission was received.

What is the product code of K013272?

The FDA product code is KLS – Enzyme Immunoassay, Theophylline, a Class II (moderate risk) device regulated under 21 CFR 862.3880.