# Lifepoint,Inc

- Location (FDA's records): Ontario, CA
- FDA decisions: 3 (1984–2004): 3 510(k) clearances
- Product codes: DJG (2), LIX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K041747: Impact Test System Saliva Test Module-Opiate (Workplace) (Nov 24, 2004)
- K041746: Impact Test System; Saliva Test Module-Opiate (Prescription Use) (Nov 23, 2004)
- K833737: CPR Locator (Aug 24, 1984)

Source page: https://510kreport.com/company/lifepoint