K252429
- 510(k) number
- K252429
- Device name
- Vektor Computational ECG Mapping System (vMap®)
- Applicant
- Vektor Medical, Inc. CA · US
- Product code
- DQK — Computer, Diagnostic, Programmable
- Decision date
- 2025-12-04
- Date received
- 2025-08-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K252429.pdf
Official FDA record: K252429
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.