# K130525: Occlusion Perfusion Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Advanced Catheter Therapies, Inc.
- Decided: Oct 3, 2013 after 217 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Indications for use
The Occlusion Perfusion catheterTM is indicated for localized infusion or irrigation of various diagnostic and therapeutic agents into the peripheral vasculature. It is not indicated for use in the neurovasculature.

Source page: https://510kreport.com/device/K130525
Methodology: https://510kreport.com/methodology