# Dms Products, Inc.

- Location (FDA's records): Flemington, NJ
- FDA decisions: 6 (1986–1989): 6 510(k) clearances
- Product codes: JSS (2), JST (1), LQL (1), JTO (1), JXA (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
- K891004: Rapidec Staph (Nov 9, 1989)
- K894805: Rapidec UR (Sep 26, 1989)
- K890626: Rapidec Coli (Jun 2, 1989)
- K890625: James Reagent (Feb 17, 1989)
- K854733: Api 20 EC (Enterobacteriaceae)(Identification Kit) (Mar 6, 1986)
- K854732: Api 50 CHB (Culture Media) (Mar 4, 1986)

Source page: https://510kreport.com/company/dms-products