# K012089: Catheffects' Desai Vectorcath Mapping System

- Pathway: 510(k) (Traditional)
- Applicant: Catheffects, LLC
- Decided: Jan 28, 2002 after 207 days
- Product code: DQK (Computer, Diagnostic, Programmable)
- Device class: 2
- Regulation: 21 CFR 870.1425
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The CATHEFFECTS Desai VectorCath™ Mapping System is intended to aid in the determination and analysis of abnarmal heart activity. The device is used in conjunction with a 5-electrode catheter to record endocardial potentials to aid in the determination of the direction of the cardiac wavefront and the possible location of the wavefront's source.

Source page: https://510kreport.com/device/K012089
Methodology: https://510kreport.com/methodology