Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K192072Substantially Equivalent

Tina-quant C-Reactive Protein IV

Roche Diagnostics Operations (Rdo), Indianapolis IN / Traditional, Substantially Equivalent

K192072 is the FDA 510(k) clearance record for Tina-quant C-Reactive Protein IV, a class II device, cleared for Roche Diagnostics Operations (Rdo) on under FDA product code DCN (System, Test, C-Reactive Protein). FDA records list 14 510(k) clearances for Roche Diagnostics Operations (Rdo), from to . As of , FDA records show no recalls naming K192072.

Clearance record

Decision date
Received
(203 days to decision)
Product code
DCN System, Test, C-Reactive Protein
Regulation
21 CFR 866.5270
Device class
Class II
Review panel
Immunology
Applicant
Roche Diagnostics Operations (Rdo) 9115 Hague Rd., Indianapolis IN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DCN

Trailing 12 months

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

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