# K914751: Selective Infusion II Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Advanced Cardiovascular Systems, Inc.
- Decided: May 24, 1993 after 580 days
- Product code: KRA (Catheter, Continuous Flush)
- Device class: 2
- Regulation: 21 CFR 870.1210
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
10 later devices descend from it; 2 cite it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K040139: Endobionics Microsyringe (Usyringe) Infusion Catheter (2004), 9 descendants of its own
- K062752: Mercator Microsyringe II Infusion Catheter (2006), 8 descendants of its own
- K140637: Peregrine System Infusion Catheter (2014), 6 descendants of its own
- K153501: Bullfrog Micro-Infusion Device (2016), 5 descendants of its own
- K161402: Bullfrog Micro-Infusion Device (2016), 4 descendants of its own

Source page: https://510kreport.com/device/K914751
Methodology: https://510kreport.com/methodology