Abbott TDM Multiconstituent Calibrator, Thermo Scientific QMS Multi-Constituent Calibrators

FDA 510(k) K120936 · Microgenics Corporation

Substantially Equivalent

510(k) numberK120936

Submission

Device name
Abbott TDM Multiconstituent Calibrator, Thermo Scientific QMS Multi-Constituent Calibrators
Applicant
Microgenics Corporation
Fremont Blvd., CA, US
Received
March 28, 2012
Decision date
December 13, 2012
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DKB – Calibrators, Drug Mixture
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3200
Specialty
Clinical Toxicology

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Questions and answers

When was Abbott TDM Multiconstituent Calibrator, Thermo Scientific QMS Multi-Constituent Calibrators cleared by the FDA?

Abbott TDM Multiconstituent Calibrator, Thermo Scientific QMS Multi-Constituent Calibrators (K120936) received a 510(k) decision of Substantially Equivalent on December 13, 2012, 260 days after the submission was received.

What is the product code of K120936?

The FDA product code is DKB – Calibrators, Drug Mixture, a Class II (moderate risk) device regulated under 21 CFR 862.3200.