# Los Alamos Diagnostics

- Location (FDA's records): Los Alamos, NM
- FDA decisions: 7 (1987–1989): 7 510(k) clearances
- Product codes: JJQ (4), JXA (3)
- 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
- K896117: Modified Model 535(TM) Luminometer (Nov 30, 1989)
- K883385: Resubmitted Utiscreen (TM) Bacterial Atp Test (Sep 7, 1988)
- K882608: Lad Model 633 Luminometer (Aug 29, 1988)
- K881439: Modified Utiscreen (TM) Bacterial Atp Test System (Apr 28, 1988)
- K874262: Lad Model 735 Luminometer (Nov 27, 1987)
- K864202: Utiscreen (R) Bacterial Atp Test (Feb 13, 1987)
- K864201: Lad Model 535 Luminometer (Jan 13, 1987)

Source page: https://510kreport.com/company/los-alamos-diagnostics