510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K960546Substantially Equivalent

Clinitek 50 Urine Chemistry Analyzer

Bayer Corp., Elkhart IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K960546 is the FDA 510(k) clearance record for CLINITEK 50 URINE CHEMISTRY ANALYZER, a class I device, cleared for Bayer Corp. on under FDA product code KQO (Automated Urinalysis System). FDA records list 20 510(k) clearances for Bayer Corp., from to . As of , FDA records show 2 recalls naming K960546.

Clearance record

Decision date
Received
(125 days to decision)
Product code
KQO Automated Urinalysis System
Regulation
21 CFR 862.2900
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Bayer Corp. 1884 Miles Ave., Elkhart IN
510(k) summary
Summary
Third party review
No

Clearances, product code KQO

Trailing 12 months

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

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