# K992379: Radionics XDC External Ventricular Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Radionics, Inc.
- Decided: Sep 8, 1999 after 54 days
- Product code: JXG (Shunt, Central Nervous System And Components)
- Device class: 2
- Regulation: 21 CFR 882.5550
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K922941 (1992). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K922941: Clinical Neuro Systems Monitorr Icp Ventricular CA, Clinical Neuro Systems, LLC (1992) Summary page 1.
- (no number) Medtronic Becker EDM Ventricular Catheters: named in the summary without a submission number

## Indications for use
As the proximal component for CSF drainage or monitoring from the lateral ventricles of the brain.

Source page: https://510kreport.com/device/K992379
Methodology: https://510kreport.com/methodology