# K000316: Meretek Ubt_Lite Breath Test for H. Pylori

- Pathway: 510(k) (Special)
- Applicant: Meretek
- Decided: Feb 24, 2000 after 23 days
- Product code: MSQ (Test, Urea (Breath Or Blood))
- Device class: 1
- Regulation: 21 CFR 866.3110
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

Source page: https://510kreport.com/device/K000316
Methodology: https://510kreport.com/methodology