# Tudor Laboratories, Inc.

- Location (FDA's records): Dallas, TX
- FDA decisions: 9 (1989–1992): 9 510(k) clearances
- Product codes: DLJ (3), LFM (1), LEG (1), LFT (1), JIS (1), LAN (1), KLI (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
- K921904: Thyroxine (Fpia) Kit (Jun 24, 1992)
- K921903: Thyroxine Calibrator Kit (May 26, 1992)
- K913240: Digitoxin (Fpia) Kit (Sep 6, 1991)
- K895572: N-Acetylprocainamide (Napa) Calibrator Kit (Oct 30, 1989)
- K895571: N-Acetylprocainamide (Napa) (Fpia) Kit (Oct 25, 1989)
- K895567: Primidone (Fpia) Kit (Oct 20, 1989)
- K895569: Valproic Acid (Fpia) Kit (Oct 3, 1989)
- K895570: Valproic Acid (Fpia) Calibrator Kit (Sep 28, 1989)

Source page: https://510kreport.com/company/tudor-laboratories