# K050130: Kerberos Proximal Solutions Rispiration System

- Pathway: 510(k) (Traditional)
- Applicant: Kerberos Proximal Solutions, Inc.
- Decided: May 13, 2005 after 112 days
- Product code: QEZ (Aspiration Thrombectomy Catheter)
- Device class: 2
- Regulation: 21 CFR 870.5150
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K904788 (1990). 38 ancestors in all.
16 later devices descend from it; 4 cite it directly.
0 of 55 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K041123: Rinspiration System,Rinspiration System Short Tip, Models FG01477/FG01703, Kerberos Proximal Solutions, Inc. (2004) Summary page 5.
- K040869: Export Catheter, Medtronic Vascular (2004) Summary page 5.
- K032763: Vascular Solutions Pronto Extraction Catheter, Vascular Solutions, Inc. (2003) Summary page 5.
- K041291: Rinspiration System, Kerberos Proximal Solutions, Inc. (2004) Summary page 5.

## Most influential descendants
- K062275: Rinspiration Catheter System, Models 50135, 550135, P7065, P70135 (2006), 9 descendants of its own
- K080901: Lbi Embolectomy System (2008), 6 descendants of its own
- K113757: Aspire Max Aspiration Catheter (2012), 5 descendants of its own
- K120508: Clearlumen Thrombectomy System (2012), 3 descendants of its own
- K140296: Clearlumen Thrombectomy System (2014), 2 descendants of its own

## Indications for use
The Kerberos Proximal Solutions Rinspiration System ig intended to infuse physician specified fluid and remove/aspirate fluid, fresh, soft emboli and thrombi from the coronary and peripheral vasculature.

Source page: https://510kreport.com/device/K050130
Methodology: https://510kreport.com/methodology