# K910372: Intimax Thrombectomy Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Applied Vascular Devices, Inc.
- Decided: Apr 26, 1991 after 87 days
- Product code: DXE (Catheter, Embolectomy)
- 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
No predicates in its family tree.
54 later devices descend from it; 1 cites it directly.
1 of 55 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K973465: Latis Graft Cleaning Catheter (1998), 53 descendants of its own
- K040010: Genesis Medical Interventional F.a.S.T. (Facilitated Aspiration/Suction Thrombectomy) Systems (2004), 51 descendants of its own
- K143563: Infusion Aspiration Catheter System (2015), 35 descendants of its own
- K092623: F.a.S.T. System Sed and CXD (2009), 7 descendants of its own
- K163549: ClotTriever Thrombectomy System (2017), 6 descendants of its own

## Recalls of this device
- Apr 17, 2024 · Class II · Z-1824-2024: The guide tip can become damaged and result in the tip detaching.

Source page: https://510kreport.com/device/K910372
Methodology: https://510kreport.com/methodology