# In Vitro Diagnostics, Inc.

- Location (FDA's records): Shelton, CT
- FDA decisions: 15 (1985–1990): 15 510(k) clearances
- Product codes: JIS (4), JIX (3), CEP (1), KHQ (1), GKZ (1), CGJ (1), JLW (1), KRZ (1), KXT (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
- K896867: Thyroid Stimulating Hormone-Eia-XT (Feb 23, 1990)
- K896866: Luteinizing Hormone-Eia-XT (Feb 13, 1990)
- K896863: Digoxin-Eia-XT (Feb 13, 1990)
- K896865: Vitro T4-Eia-XT (Jan 30, 1990)
- K896925: T Uptake Enzyme Immunoassay Crimped Tube Kit (Jan 18, 1990)
- K896864: Follicle Stimulating Hormone-Eia-XT (Jan 11, 1990)
- K873832: Reagents for Use on Contraves DC300, DC500, AL801 (Nov 23, 1987)
- K871187: Lithium Internal Standard 3000 Meq/L #60084 (May 28, 1987)

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