Vektor Medical Receives FDA Clearance for vMap™, First Technology Designed to Identify Arrhythmia Hot Spots Anywhere in Heart in Minutes Using Only ECG Data

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Non-Invasive Technology Requires No Vests, CT or MRI Imaging, or Invasive Mapping

SAN DIEGO–(BUSINESS WIRE)–Vektor Medical, Inc. today announced U.S. Food and Drug Administration (FDA) 510(k) clearance for its novel computational ECG mapping system, vMap™. vMap is designed to map potential arrhythmia sources (hot spots) associated with stable or unstable arrhythmias anywhere in the heart – including all four chambers, the septal wall, and the outflow tracts – in less than three minutes using only ECG data, to improve outcomes in ablation procedures. Following clearance, the vMap system will be commercially available to sites across the U.S.

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