510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K030768Substantially Equivalent

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

Cliniqa Corporation, Fallbrook CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K030768 is the FDA 510(k) clearance record for CLINIQA LIQUID QC CARDIAC MARKER CONTROL LEVELS 1, 2 & 3, TRI-LEVEL, a class I device, cleared for Cliniqa Corporation on under FDA product code JJT (Enzyme Controls (Assayed And Unassayed)). FDA records list 36 510(k) clearances for Cliniqa Corporation, from to . As of , FDA records show one recall naming K030768.

Clearance record

Decision date
Received
(10 days to decision)
Product code
JJT Enzyme Controls (Assayed And Unassayed)
Regulation
21 CFR 862.1660
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Cliniqa Corporation 1432 S. Mission Rd., Fallbrook CA
510(k) summary
Statement
Third party review
No

Clearances, product code JJT

Trailing 12 months

FDA records hold no clearances under product code JJT in the trailing twelve months.

FDA records show no clearances under product code JJT in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code JJT, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260