Diazyme Lipoprotein (a) Calibrator Set, Control Set

FDA 510(k) K131556 · Diazyme Laboratories

Substantially Equivalent

510(k) numberK131556

Submission

Device name
Diazyme Lipoprotein (a) Calibrator Set, Control Set
Applicant
Diazyme Laboratories
Poway, CA, US
Received
May 29, 2013
Decision date
June 26, 2013
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary 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 Diazyme Lipoprotein (a) Calibrator Set, Control Set cleared by the FDA?

Diazyme Lipoprotein (a) Calibrator Set, Control Set (K131556) received a 510(k) decision of Substantially Equivalent on June 26, 2013, 28 days after the submission was received.

What is the product code of K131556?

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