# DEN130005: Quantitation of Organophosphate  Metabolites in Urine by LC/MS/MS

- Pathway: De Novo (Post-NSE)
- Applicant: Centers for Disease Control and Prevention
- Decided: Aug 8, 2013 after 72 days
- Product code: PDY (Organophosphate Test System)
- Device class: 2
- Regulation: 21 CFR 862.3652
- 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. De Novo decisions do not claim a predicate device.

Source page: https://510kreport.com/device/DEN130005
Methodology: https://510kreport.com/methodology