# K050794: Angiojet DVX Rheolytic Thrombectomy Catheter

- Pathway: 510(k) (Special)
- Applicant: Possis Medical, Inc.
- Decided: Apr 28, 2005 after 30 days
- Product code: QEZ (Aspiration Thrombectomy Catheter)
- Device class: 2
- Regulation: 21 CFR 870.5150
- Recalls of this device: 1 (0 Class I)
- 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.
34 later devices descend from it; 1 cites it directly.
1 of 43 devices in its family (counting itself) has 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
- K072269: Angiojet Ultra DVX Thrombectomy Set, Model: 106552 (2007), 33 descendants of its own
- K090253: Angiojet Ultra DVX Thrombectomy Set, Model 106552-001, Angiojet Ultra Xpeedior Thrombectomy Set, Model 105040-001 (2009), 32 descendants of its own
- K091593: Angio Jet Ultra DVX and Xpeedior Thrombectomy Sets (2009), 31 descendants of its own
- K101406: Angiojet Solent Proxi Thrombectomy Set Model 109676-001 (2010), 30 descendants of its own
- K111182: Angiojet Solent Omni Thrombectomy Set (2011), 28 descendants of its own

## Recalls of this device
- Jun 19, 2007 · Not classified · Z-1131-2007: Mislabeling : Possis AngioJet XVG Catheter Thrombectomy Sets display incorrect information on the outer packaging box and also on the inner sterile tray. The labeling incorrectly states that the unit 

## Indications for use
The AngioJet DVX Rheolytic Thrombectomy Catheter is intended for use with the AngioJet System in breaking apart and removing thrombus from infra-inguinal peripheral arteries > 3 mm in diameter.

Source page: https://510kreport.com/device/K050794
Methodology: https://510kreport.com/methodology