# K191305: Hereaeus Poseidon Microcatheter

- Pathway: 510(k) (Traditional)
- Applicant: Heraeus Medical Components, LLC
- Decided: Dec 19, 2019 after 219 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 K060224 (2006). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K131772: Cantata (R) 2.9 Microcatheter, Cook, Inc. (2014) Summary page 4.

## Indications for use
The Poseidon Microcatheter is intended for use in peripheral and coronary vessels for diagnostic and interventional procedures including small or superselective anatomy.

Source page: https://510kreport.com/device/K191305
Methodology: https://510kreport.com/methodology