UniCel DxC SYNCHRON System HDL Cholesterol reagent(HDL),Unicel DxC SYNCHRON System HDL Calibrator

FDA 510(k) K142985 · Beckman Coulter, Inc.

Substantially Equivalent

510(k) numberK142985

Submission

Device name
UniCel DxC SYNCHRON System HDL Cholesterol reagent(HDL),Unicel DxC SYNCHRON System HDL Calibrator
Applicant
Beckman Coulter, Inc.
Brea, CA, US
Received
October 16, 2014
Decision date
February 26, 2015
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JIT – Calibrator, Secondary
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1150
Specialty
Clinical Chemistry

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Questions and answers

When was UniCel DxC SYNCHRON System HDL Cholesterol reagent(HDL),Unicel DxC SYNCHRON System HDL Calibrator cleared by the FDA?

UniCel DxC SYNCHRON System HDL Cholesterol reagent(HDL),Unicel DxC SYNCHRON System HDL Calibrator (K142985) received a 510(k) decision of Substantially Equivalent on February 26, 2015, 133 days after the submission was received.

What is the product code of K142985?

The FDA product code is JIT – Calibrator, Secondary, a Class II (moderate risk) device regulated under 21 CFR 862.1150.