# K954059: Titan 20 CC Driver

- Pathway: 510(k) (Traditional)
- Applicant: I-Flow Corp.
- Decided: Sep 29, 1995 after 31 days
- Product code: MEB (Pump, Infusion, Elastomeric)
- Device class: 2
- Regulation: 21 CFR 880.5725
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K972173: Medi-Sis Syringe Infusion System (1997), 1 descendant of its own
- K111381: Medi-Sis Syringe Infusion System (2012), 0 descendants of its own

Source page: https://510kreport.com/device/K954059
Methodology: https://510kreport.com/methodology