# K051526: Uritek-720+ Urine Analyzer

- Pathway: 510(k) (Traditional)
- Applicant: Teco Diagnostics
- Decided: Aug 16, 2005 after 69 days
- Product code: KQO (Automated Urinalysis System)
- Device class: 1
- Regulation: 21 CFR 862.2900
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K141289: TC-Thunderbolt Automated Urine Analyzer System and TC-Thunderbolt Urs-10 Strips (2015), 0 descendants of its own

## Indications for use
The Uritek-720+ Urine Analyzer is intended for use with Teco Urine Reagent Strips for Urinalysis such as URS-10, used in the determination of glucose, protein, pH. bilirubin, blood. ketone, urobilinogen, nitrite, specific gravity, and leukocytes in urine.

Source page: https://510kreport.com/device/K051526
Methodology: https://510kreport.com/methodology