510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K141925Substantially Equivalent

Total Protein Urine/csf Gen.3

Roche Diagnostics Operations (Rdo), Indianapolis IN / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K141925 is the FDA 510(k) clearance record for TOTAL PROTEIN URINE/CSF GEN.3, a class I device, cleared for Roche Diagnostics Operations (Rdo) on under FDA product code JIQ (Turbidimetric Method, Protein Or Albumin (Urinary, Non-Quant.)). FDA records list 14 510(k) clearances for Roche Diagnostics Operations (Rdo), from to . As of , FDA records show no recalls naming K141925.

Clearance record

Decision date
Received
(146 days to decision)
Product code
JIQ Turbidimetric Method, Protein Or Albumin (Urinary, Non-Quant.)
Regulation
21 CFR 862.1645
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Roche Diagnostics Operations (Rdo) 9115 Hague Rd., Indianapolis IN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JIQ

Trailing 12 months

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

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