# K993564: Possis Angiojet X-Stream Rheolytic Thrombectomy Catheter, Model 103587-002

- Pathway: 510(k) (Traditional)
- Applicant: Possis Medical, Inc.
- Decided: Apr 28, 2000 after 190 days
- Product code: MCW (Catheter, Peripheral, Atherectomy)
- Device class: 2
- Regulation: 21 CFR 870.4875
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
94 later devices descend from it; 5 cite it directly.
4 of 95 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) AngioJet LF140 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 XPEEDIOR Rheolytic™ Thrombectomy Catheter is intended for breaking apart and removing thrombus from A-V access conduits when used with the AngioJet System.

Source page: https://510kreport.com/device/K993564
Methodology: https://510kreport.com/methodology