Bayer Special Chemistry Controls

FDA 510(k) K033379 · Bayer Diagnostics Corp.

Substantially Equivalent

510(k) numberK033379

Submission

Device name
Bayer Special Chemistry Controls
Applicant
Bayer Diagnostics Corp.
Tarrytown, NY, US
Received
October 22, 2003
Decision date
December 19, 2003
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JJY – Multi-Analyte Controls, All Kinds (Assayed)
Device class
Class I (low risk)
Regulation
21 CFR 862.1660
Specialty
Clinical Chemistry

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More from Aalto Scientific, Ltd.

510(k)DeviceDecision
K033380Bayer Special Chemistry CalibratorsJIX · Abbreviated 12/16/2003SE
K033007Bayer Advia Digoxin Assay for the Integrated Module SystemKXT · Traditional 11/14/2003SE
K031857Advia Chemistry ALPHA-1 Antitrypsin AssayDEM · Traditional 09/04/2003SE
K022096Uric Acid Assay for the Advia Integrated Modular SystemKNK · Traditional 03/18/2003SE
K030452Bayer Ligand Plus 1, 2, 3 ControlsJJY · Abbreviated 03/03/2003SE
K023840Acid Phosphatase Assay for the Advia 1650CKB · Traditional 01/07/2003SE
K023841Ammonia Assay for the Advia 1650JIF · Traditional 12/24/2002SE
K022177Prostate Specific Antigen (Psa) Assay for the Advia Integrated Modular SystemLTJ · Traditional 12/17/2002SE
K022329Ca 125 II Assay for the Bayer Advia Integrated Module SystemLTK · Traditional 11/27/2002SE
K023184Ethanol Assay for the Bayer Advia Integrated Module SystemDIC · Traditional 11/18/2002SE

Questions and answers

When was Bayer Special Chemistry Controls cleared by the FDA?

Bayer Special Chemistry Controls (K033379) received a 510(k) decision of Substantially Equivalent on December 19, 2003, 58 days after the submission was received.

What is the product code of K033379?

The FDA product code is JJY – Multi-Analyte Controls, All Kinds (Assayed), a Class I (low risk) device regulated under 21 CFR 862.1660.