# Caesarea Medical Electronics, Ltd.

- Location (FDA's records): Caesarea, IL
- FDA decisions: 9 (2003–2008): 9 510(k) clearances
- Product codes: FRN (8), LZH (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 48 (39 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Q Core Medical, Ltd.: 2 (https://510kreport.com/company/q-core-medical)
- Iradimed Corporation: 1 (https://510kreport.com/company/iradimed)
- Q-Core, Ltd.: 1 (https://510kreport.com/company/q-core)

## Its most-cited devices
- K060479: Modification to Bodyguard Infusion Pump System (2006), cited by 2
- K031749: Bodyguard Infusion System (2003), cited by 2

## Recent decisions
- K080954: T34L Syringe Driver (May 16, 2008)
- K070235: Bodyguard Pain Manager Infusion  System (May 18, 2007)
- K070718: Modification to: Bodyguard Infusion System (Apr 13, 2007)
- K061325: Bodygaurd Pain Manager Infusion System (Aug 24, 2006)
- K060479: Modification to Bodyguard Infusion Pump System (May 12, 2006)
- K050800: Niki T34 and Bodyguard T34 Syringe Drivers (Nov 23, 2005)
- K042696: Bodyguard Infusion Pump System (Mar 11, 2005)
- K040957: Noa Iii Enteral Nutrition Pump (May 21, 2004)

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