# K183403: JETi 88 Peripheral Thrombectomy System

- Pathway: 510(k) (Traditional)
- Applicant: Walk Vascular, LLC
- Decided: Apr 17, 2019 after 131 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
No predicates in its family tree.
4 later devices descend from it; 2 cite it directly.
0 of 5 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 no predicate by number.

## Most influential descendants
- K201998: JETi AIO Peripheral Thrombectomy System (2020), 2 descendants of its own
- K213565: JETi AIO Peripheral Thrombectomy System (2022), 1 descendant of its own
- K232458: JETi™Hydrodynamic Thrombectomy System (2023), 0 descendants of its own
- K192439: JETi Peripheral Thrombectomy System (2019), 0 descendants of its own

Source page: https://510kreport.com/device/K183403
Methodology: https://510kreport.com/methodology