Abbott Lipid Multi Constituent Calibrator

FDA 510(k) K123372 · Abbott Laboratories

Substantially Equivalent

510(k) numberK123372

Submission

Device name
Abbott Lipid Multi Constituent Calibrator
Applicant
Abbott Laboratories
Irving, TX, US
Received
November 1, 2012
Decision date
January 14, 2013
Decision
Substantially Equivalent (SESE)
Type
Traditional 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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Questions and answers

When was Abbott Lipid Multi Constituent Calibrator cleared by the FDA?

Abbott Lipid Multi Constituent Calibrator (K123372) received a 510(k) decision of Substantially Equivalent on January 14, 2013, 74 days after the submission was received.

What is the product code of K123372?

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