# K192625: PG Pro Microcatheter

- Pathway: 510(k) (Traditional)
- Applicant: MicroVention, Inc. A TERUMO Group Company
- Decided: Nov 21, 2019 after 59 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K960806 (1996). 8 ancestors in all.
3 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)
- K142449: Headway 27 Microcatheter, MicroVention, Inc. (2015) Summary page 4.

## Most influential descendants
- K231600: SENDERO Microcatheter (2023), 2 descendants of its own
- K240384: SENDERO Microcatheter (2024), 1 descendant of its own
- K242644: SENDERO MAX Delivery Catheter (2024), 0 descendants of its own

## Indications for use
The PG Pro microcatheter is intended for the peripheral vasculature for the infusion of diagnostic and therapeutic agents.

Source page: https://510kreport.com/device/K192625
Methodology: https://510kreport.com/methodology