# K062275: Rinspiration Catheter System, Models 50135, 550135, P7065, P70135

- Pathway: 510(k) (Special)
- Applicant: Kerberos Proximal Solutions, Inc.
- Decided: Sep 20, 2006 after 44 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: 6 generations back to K904788 (1990). 39 ancestors in all.
9 later devices descend from it; 3 cite it directly.
0 of 49 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K050130: Kerberos Proximal Solutions Rispiration System, Kerberos Proximal Solutions, Inc. (2005) Summary page 5.

## Most influential descendants
- K080901: Lbi Embolectomy System (2008), 6 descendants of its own
- K113757: Aspire Max Aspiration Catheter (2012), 5 descendants of its own
- K220780: ROVO Mechanical Thrombectomy Device (2023), 1 descendant of its own
- K200871: Aspire MAX 7 - 11F Mechanical Thrombectomy System and Aspire Mechanical Aspirator (2020), 1 descendant of its own
- K253730: RoVo Mechanical Thrombectomy System (2026), 0 descendants of its own

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

Source page: https://510kreport.com/device/K062275
Methodology: https://510kreport.com/methodology