Bayer Special Chemistry Calibrators

FDA 510(k) K033380 · Bayer Diagnostics Corp.

Substantially Equivalent

510(k) numberK033380

Submission

Device name
Bayer Special Chemistry Calibrators
Applicant
Bayer Diagnostics Corp.
Tarrytown, NY, US
Received
October 22, 2003
Decision date
December 16, 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
JIX – Calibrator, Multi-Analyte Mixture
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1150
Specialty
Clinical Chemistry

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K023840Acid Phosphatase Assay for the Advia 1650CKB · Traditional 01/07/2003SE
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K022177Prostate Specific Antigen (Psa) Assay for the Advia Integrated Modular SystemLTJ · Traditional 12/17/2002SE
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Questions and answers

When was Bayer Special Chemistry Calibrators cleared by the FDA?

Bayer Special Chemistry Calibrators (K033380) received a 510(k) decision of Substantially Equivalent on December 16, 2003, 55 days after the submission was received.

What is the product code of K033380?

The FDA product code is JIX – Calibrator, Multi-Analyte Mixture, a Class II (moderate risk) device regulated under 21 CFR 862.1150.