# Symbios Medical Products, LLC

- Location (FDA's records): Indianapolis, IN
- FDA decisions: 3 (2005–2007): 3 510(k) clearances
- Product codes: MEB (3)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 1 (1 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Its most-cited devices
- K051474: Symbios Disposable Infusion Pump Kit (2005), cited by 1

## Recent decisions
- K072921: Disposable Infusion Pump Kit, GO Pump Rapid Recovery System (Nov 26, 2007)
- K071735: Modification to Disposable Infusion Pump Kit (Jul 19, 2007)
- K051474: Symbios Disposable Infusion Pump Kit (Jul 1, 2005)

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