# Elite Diagnostic, Ltd.

- Location (FDA's records): Indianapolis, IN
- FDA decisions: 5 (1989–1989): 5 510(k) clearances
- Product codes: GFO (2), GIZ (1), GGL (1), GJS (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
- K890859: Edl Global Activated Partial Thromboplastin Time (Apr 21, 1989)
- K891370: Edl One-Stage Prothrombin Time Reagent (Apr 21, 1989)
- K891179: Edl Normal Coagulation Control (Apr 10, 1989)
- K891175: Edl Abnormal Coagulation Control (Apr 10, 1989)
- K890619: Edl Activated Partial Thromboplastin Time Reagent (Mar 15, 1989)

Source page: https://510kreport.com/company/elite-diagnostic