# K901074: Code #94315 Retrograde Coronary Sinus Perf Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Dlp, Inc.
- Decided: Jul 6, 1990 after 120 days
- Product code: DWF (Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass)
- Device class: 2
- Regulation: 21 CFR 870.4210
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 3 cite it directly.
0 of 5 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
- K030696: Retrograde Coronary Sinus Perfusion Cannula with NO Pressure Line (15 French, Manual and Auto Inflate) (2003), 2 descendants of its own
- K132995: DLP Retrograde Coronary Sinus Perfusion Cannula Without Pressure Monitoring Line, DLP Retrograde Coronary Sinus Perfusio (2013), 0 descendants of its own
- K123762: DLP Retrograde Coronary Sinus Perfusion Cannula with Auto-Inflate Cuff (2013), 0 descendants of its own
- K090869: Mircsp (Minimally Invasive Retrograde Coronary Sinus Perfusion) Manual Inflate Cannula, Model 94113TD (2009), 0 descendants of its own

Source page: https://510kreport.com/device/K901074
Methodology: https://510kreport.com/methodology