# K992934: Lemaitre Venous Thrombectomy Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Vascutech, Inc.
- Decided: Mar 1, 2000 after 183 days
- Product code: DXE (Catheter, Embolectomy)
- 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.
11 later devices descend from it; 1 cites it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K070403: Pronto .035 Extraction Catheter (2007), 10 descendants of its own
- K110315: Nexgen Peripheral Mechanical Retrieval Device (2011), 6 descendants of its own
- K192814: Pounce Thrombus Retrieval System (2020), 5 descendants of its own
- K211492: Pounce Thrombectomy System (2021), 4 descendants of its own
- K220501: Pounce Thrombectomy System (2022), 3 descendants of its own

## Indications for use
The LeMaitre Venous Thrombectomy Catheter is indicated for the removal of venous thrombi.

Source page: https://510kreport.com/device/K992934
Methodology: https://510kreport.com/methodology