# Pb Diagnostics, Inc.

- Location (FDA's records): Westwood, MA
- FDA decisions: 4 (1991–1993): 4 510(k) clearances
- Product codes: MJX (1), LKQ (1), LFX (1), LGD (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
- K925703: Opus Serology Controls (Apr 8, 1993)
- K921523: Opus (R) Toxo-G Test System (Sep 14, 1992)
- K915870: Opus Rubella Test System (Mar 23, 1992)
- K913080: Opus (R) Anti CMV-M (Oct 28, 1991)

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