# K914995: Cordis Straight Ventricular Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Cordis Corp.
- Decided: Mar 9, 1992 after 123 days
- Product code: JXG (Shunt, Central Nervous System And Components)
- Device class: 2
- Regulation: 21 CFR 882.5550
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K955265: Cordis Sharp-Ended Stylet; Blunt-Ended Stylet; Cyst Puncture Catheter (1996), 0 descendants of its own

## Recalls of this device
- Aug 23, 2016 · Class II · Z-2909-2016: During final sampling inspection, one of the lots was discovered with a total incomplete packaging seal of the sterile product.

Source page: https://510kreport.com/device/K914995
Methodology: https://510kreport.com/methodology