# K170223: Progreat

- Pathway: 510(k) (Traditional)
- Applicant: Ashitaka Factory of Terumo Corporation
- Decided: Jul 21, 2017 after 177 days
- Product code: DQO (Catheter, Intravascular, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 870.1200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K915414 (1992). 3 ancestors in all.
1 later device descends from it; 1 cites 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)
- K033583: Progreat, Terumo Medical Corp. (2003) Summary page 6.

## Most influential descendants
- K232536: Soldier Microcatheter (2024), 0 descendants of its own

## Indications for use
The Progreat is intended for the infusion of contrast media into all peripheral vessels up to and including the cervical vessels, all vessels in the lower and upper extremities, and all coronary vessels. The Progreat is also intended for drug infusion in intra-arterial therapy and the infusion of embolic materials for hemostasis. The Progreat should not be used in cerebral vessels.

Source page: https://510kreport.com/device/K170223
Methodology: https://510kreport.com/methodology