# K082382: Angiojet Ultra Avx Thrombectomy Set, Model 105039

- Pathway: 510(k) (Traditional)
- Applicant: Possis Medical, Inc.
- Decided: Dec 12, 2008 after 115 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). 5 ancestors in all.
34 later devices descend from it; 2 cite it directly.
1 of 40 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K073441: Angiojet Ultra Avx Thrombectomy Set, Model 105039, Possis Medical, Inc. (2008) Summary page 5.

## Most influential descendants
- 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
- K151313: ZelanteDVT Thrombectomy Set (2015), 26 descendants of its own

## Indications for use
The AngioJet Ultra AVX Thrombectomy Set is intended for use with the AngioJet Ultra System in breaking apart and removing thrombus from A-V access conduits> 3 mm in diameter.

Source page: https://510kreport.com/device/K082382
Methodology: https://510kreport.com/methodology