# Squibb Diagnostics

- Location (FDA's records): New Brunswick, NJ
- FDA decisions: 3 (1983–1989): 3 510(k) clearances
- Product codes: FRN (2), HAM (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
- K883609: Acces. Package for Use W/Cardiogen-82 Generator (Apr 14, 1989)
- K842568: Radionuclide Infusion System (Oct 19, 1984)
- K823755: Biceps Electrocautery System (Jan 26, 1983)

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