# K972610: Possis Angiojet Rapid Thombectomy Catheters--F105 Catheter Model 3030C, LF140 Catheter Model 3040C

- Pathway: 510(k) (Traditional)
- Applicant: Possis Medical, Inc.
- Decided: Apr 11, 2000 after 1,002 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: 2 generations back to K901627 (1990). 2 ancestors in all.
81 later devices descend from it; 6 cite it directly.
4 of 84 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K901627: Arterial Embolectomy Catheter, Applied Vascular Devices, Inc. (1990) Summary page 5.
- K960970: Possis Angiojet Rapid Thrombectomy  Catheter System, F105 Catheter,Model 3030C,LF140 Catheter,Model 3040C,Pump Set 3020P, Possis Medical, Inc. (1996) Summary page 5.
- (no number) Fogarty Arterial Embolectomy Catheter: named in the summary without a submission number

## Most influential descendants
- K040013: Angiojet Xpeedior 120 Catheter and Angiojet Power Pulse Spray Ancillary Kit (2004), 70 descendants of its own
- K052256: Angiojet Xpeedior 120 Catheter (2005), 68 descendants of its own
- 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
- K073441: Angiojet Ultra Avx Thrombectomy Set, Model 105039 (2008), 35 descendants of its own

## Indications for use
The AngioJet System, with the Catheter, is intended for breaking apart and removing thrombotic obstructions from infra-inguinal peripheral arteries > 2.0 mm in diameter

Source page: https://510kreport.com/device/K972610
Methodology: https://510kreport.com/methodology