# K211546: Vektor Computational ECG Mapping System (vMap)

- Pathway: 510(k) (Traditional)
- Applicant: Vektor Medical, Inc.
- Decided: Nov 9, 2021 after 174 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). 30 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 32 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K201298: VX1, Volta Medical (2020) Summary page 5.
- K181918: CardioInsight Cardiac Mapping System, Medtronic, Inc. (2018) Summary page 5.

## Most influential descendants
- K252429: Vektor Computational ECG Mapping System (vMap®) (2025), 0 descendants of its own

## Indications for use
The Vektor Computational ECG Mapping System (vMap™) is intended for the analysis, display, and storage of cardiac electrophysiological data and maps for analysis by a physician.

Source page: https://510kreport.com/device/K211546
Methodology: https://510kreport.com/methodology