# K002254: Cook Pressure Monitoring Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Cook, Inc.
- Decided: Mar 16, 2001 after 234 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
No predicates in its family tree.
14 later devices descend from it; 3 cite it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K151821: ER-REBOA Catheter (2015), 9 descendants of its own
- K170411: ER-REBOA Catheter (2017), 8 descendants of its own
- K172790: ER-REBOA Catheter (2017), 4 descendants of its own
- K180846: Arterial Pressure Monitoring Set/Tray (2018), 2 descendants of its own
- K180792: Arterial Pressure Monitoring Set/Tray (2018), 2 descendants of its own

Source page: https://510kreport.com/device/K002254
Methodology: https://510kreport.com/methodology