# K200313: VIVO

- Pathway: 510(k) (Traditional)
- Applicant: Catheter Precision, Inc.
- Decided: Sep 14, 2020 after 221 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
Longest line of descent: 10 generations back to K000248 (2000). 17 ancestors in all.
No later device cites it as a predicate yet.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K183195: VIVO, Catheter Precision, Inc. (2019) Summary page 5.

## Indications for use
VIVO is intended for acquisition, analysis, display and storage of cardiac electrophysiological data and maps for analysis by a physician. VIVO is intended to be used as a pre-procedure planning tool for patients with structurally normal hearts undergoing ablation treatment for idiopathic ventricular arrhythmias.

Source page: https://510kreport.com/device/K200313
Methodology: https://510kreport.com/methodology