# K052256: Angiojet Xpeedior 120 Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Possis Medical, Inc.
- Decided: Nov 10, 2005 after 84 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: 4 generations back to K901627 (1990). 8 ancestors in all.
68 later devices descend from it; 6 cite it directly.
4 of 77 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K040013: Angiojet Xpeedior 120 Catheter and Angiojet Power Pulse Spray Ancillary Kit, Possis Medical, Inc. (2004) Summary page 5.

## Most influential descendants
- K061951: Angiojet Xpeedior Rheolytic Thrombectomy Catheter, Model Xpeedior 120 (2006), 66 descendants of its own
- K071514: Angiojet Xpeedior Rheolytic Thrombectomy Catheter, Model 104307 (2007), 63 descendants of its own
- K071342: Angiojet Ultra Xpeedior Thrombectomy Set, Model 105040, 105042, 106552, 105043, 105041, 106553, 105039 (2007), 34 descendants of its own
- K072269: Angiojet Ultra DVX Thrombectomy Set, Model: 106552 (2007), 33 descendants of its own
- K071336: Angiojet Xpeedior Rheolytic Thrombectomy Catheter, Model 104307 (2007), 33 descendants of its own

## Indications for use
The AngioJet Xpeedior 120 Catheter is intended for use with the AngioJet System in breaking apart and removing thrombus from infrainguinal peripheral arteries >3.0 mm in diameter; and/or with the AngioJet Power Pulse Kit for the control and selective infusion of physician specified fluids, including thrombolytic agents, into the peripheral vascular system.

Source page: https://510kreport.com/device/K052256
Methodology: https://510kreport.com/methodology