# K992965: Cordis Webster Fixed Curve Catheters, Models D-1124, D-1085

- Pathway: 510(k) (Traditional)
- Applicant: Cordis Webster, Inc.
- Decided: Nov 26, 1999 after 85 days
- Product code: DRF (Catheter, Electrode Recording, Or Probe, Electrode Recording)
- Device class: 2
- Regulation: 21 CFR 870.1220
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
8 later devices descend from it; 3 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K012708: Electrophysiology Catheter (2002), 5 descendants of its own
- K043393: Reprocessed EP Technologies Electrophysiology Catheters (2005), 1 descendant of its own
- K201445: MultiCath, AcQRate Dx Fixed Curve Catheter (2021), 0 descendants of its own
- K052414: Reprocessed Electrophysiology Catheter (2005), 0 descendants of its own
- K052603: Reprocessed Daig Livewire Electrophysiology Catheters (2005), 0 descendants of its own

## Indications for use
The Cordis Webster Fixed Curve Catheter is indicated for electrophysiology mapping of cardiac structures in adults and children 4 years of age and older; i.e. stimulation and recording only.

Source page: https://510kreport.com/device/K992965
Methodology: https://510kreport.com/methodology