# Sensititre, Ltd.

- Location (FDA's records): Westlake, OH
- FDA decisions: 3 (1988–1996): 3 510(k) clearances
- Product codes: JWY (2), LRG (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: 9 (9 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K960220: Sensititre 18 Hour Susceptibility Plates (Mar 11, 1996)
- K911419: Sensititre Aris Module (Jul 1, 1992)
- K880641: Sensititre Stability Plates (May 13, 1988)

Source page: https://510kreport.com/company/sensititre