510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K051526Substantially Equivalent

Uritek-720+ Urine Analyzer

Teco Diagnostics, Anaheim CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K051526 is the FDA 510(k) clearance record for URITEK-720+ URINE ANALYZER, a class I device, cleared for Teco Diagnostics on under FDA product code KQO (Automated Urinalysis System). FDA records list 55 510(k) clearances for Teco Diagnostics, from to . As of , FDA records show no recalls naming K051526.

Clearance record

Decision date
Received
(69 days to decision)
Product code
KQO Automated Urinalysis System
Regulation
21 CFR 862.2900
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Teco Diagnostics 1268 N Lakeview Ave., Anaheim CA
510(k) summary
Statement
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