# Florence Medical, Ltd.

- Location (FDA's records): Ra'Ananna  43373, IL
- FDA decisions: 3 (2001–2002): 3 510(k) clearances
- Product codes: DQK (2), DSK (1)
- Predicates its devices cite: 3 (3 its own); citations of its devices by later devices: 4 (3 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Radi Medical Systems AB: 1 (https://510kreport.com/company/radi-medical-systems)

## Its most-cited devices
- K003122: Smartflow, Model Sfip 2000 (2001), cited by 2
- K020127: Smartflow Pulse Transmission Coefficient (2002), cited by 1
- K012947: Smartflow (2001), cited by 1

## Recent decisions
- K020127: Smartflow Pulse Transmission Coefficient (Feb 14, 2002)
- K012947: Smartflow (Oct 2, 2001)
- K003122: Smartflow, Model Sfip 2000 (May 14, 2001)

Source page: https://510kreport.com/company/florence-medical