# K214025: PROWLER SELECT LP ES Microcatheter; PROWLER XS Microcatheter

- Pathway: 510(k) (Special)
- Applicant: Medos International SARL
- Decided: Apr 12, 2022 after 111 days
- Product code: KRA (Catheter, Continuous Flush)
- Device class: 2
- Regulation: 21 CFR 870.1210
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K945904 (1995). 8 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K021591: Prowler Select (10, 14, and Plus) Infusion Catheters with and Without Pre-Shaped Tips, Cordis Neurovascular, Inc. (2002) Summary page 4.

## Most influential descendants
- K223139: Wallaby 017 Micro Catheter (2023), 0 descendants of its own

## Indications for use
The PROWLER SELECT LP ES Microcatheter is intended for the introduction of embolic devices and infusion of diagnostic agents into the peripheral and neuro vasculature. The PROWLER XS Microcatheter is intended for the introduction of embolic devices and infusion of diagnostic agents into the peripheral and neuro vasculature.

Source page: https://510kreport.com/device/K214025
Methodology: https://510kreport.com/methodology