# K191442: Campylobacter Chek

- Pathway: 510(k) (Special)
- Applicant: Techlab, Inc.
- Decided: Jun 20, 2019 after 21 days
- Product code: LQP (Campylobacter Spp.)
- 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’s file for it is a 510(k) statement, which names no predicate.

Source page: https://510kreport.com/device/K191442
Methodology: https://510kreport.com/methodology