Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K973869Substantially Equivalent

Trace Reagent Line for the Cobas Mira

Trace America, Inc., Miami FL / Traditional, Substantially Equivalent

K973869 is the FDA 510(k) clearance record for TRACE REAGENT LINE FOR THE COBAS MIRA, a class I device, cleared for Trace America, Inc. on under FDA product code CKA (Nadh Oxidation/Nad Reduction, Alt/Sgpt). FDA records list 22 510(k) clearances for Trace America, Inc., from to . As of , FDA records show no recalls naming K973869.

Clearance record

Decision date
Received
(105 days to decision)
Product code
CKA Nadh Oxidation/Nad Reduction, Alt/Sgpt
Regulation
21 CFR 862.1030
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Trace America, Inc. 7260 NW 58th St., Miami FL
510(k) summary
Statement
Third party review
No

Clearances, product code CKA

Trailing 12 months

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

FDA records show no clearances under product code CKA in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code CKA, 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