Cliniqa Liquid QC Cardiac Marker Control Levels 1, 2 & 3, Tri-Level

FDA 510(k) K030768 · Cliniqa Corporation

Substantially Equivalent

510(k) numberK030768

Submission

Device name
Cliniqa Liquid QC Cardiac Marker Control Levels 1, 2 & 3, Tri-Level
Applicant
Cliniqa Corporation
Fallbrook, CA, US
Received
March 11, 2003
Decision date
March 21, 2003
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JJT – Enzyme Controls (Assayed And Unassayed)
Device class
Class I (low risk)
Regulation
21 CFR 862.1660
Specialty
Clinical Chemistry

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Questions and answers

When was Cliniqa Liquid QC Cardiac Marker Control Levels 1, 2 & 3, Tri-Level cleared by the FDA?

Cliniqa Liquid QC Cardiac Marker Control Levels 1, 2 & 3, Tri-Level (K030768) received a 510(k) decision of Substantially Equivalent on March 21, 2003, 10 days after the submission was received.

What is the product code of K030768?

The FDA product code is JJT – Enzyme Controls (Assayed And Unassayed), a Class I (low risk) device regulated under 21 CFR 862.1660.