# K161731: Cleveland Multiport Ventricular Catheter Set

- Pathway: 510(k) (Traditional)
- Applicant: Parker Hannifin Corp.
- Decided: Mar 27, 2017 after 277 days
- Product code: HCA (Catheter, Ventricular)
- Device class: 2
- Regulation: 21 CFR 882.4100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K102101 (2011). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K123605: Smartflow Catheter, Mri Interventions, Inc. (2013) Summary page 4.
- K150660: Alcyone MEMS Cannula (AMC) System, Alcyone Lifesciences, Inc. (2015) Summary page 6.
- K102101: Surgivision MR Compatible Ventricular Cannula, Surgivision, Inc. (2011) Summary page 6.

## Indications for use
The Cleveland Multiport Ventricular Catheter Set is indicated for gaining access to the ventricles of the brain for the removal of cerebrospinal fluid (CSF) or for injecting Cytarabine.

Source page: https://510kreport.com/device/K161731
Methodology: https://510kreport.com/methodology