510(k) K252429

Device
Vektor Computational ECG Mapping System (vMap®)
Applicant
Vektor Medical, Inc.
510(k) number
K252429
Product code
DQK
Decision
Substantially Equivalent (SESE)
Decision date
2025-12-04
Date received
2025-08-01
Regulation
870.1425
Classification name
Computer, Diagnostic, Programmable
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Mihir Naik
Address
9255 Towne Centre Dr. Suite 840 San Diego CA US 92121 92121

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Other 510(k) Records For Product Code DQK

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K253861ACORYS MAPPING SYSTEMCorify Care S.L2026-04-13
K253473SynchronyStereotaxis, Inc.2026-04-01
K253186HemoSphere Nano Monitor (HSNANO1)Edwards Lifesciences, LLC2026-02-24
K252972CARTO™ 3 EP Navigation System V8.4Biosense Webster, Inc.2026-02-20
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K251591Holter ECG and ABP system (HolterABP)Edan Instruments, Inc.2026-02-09
K251218SafeBeat Rx AppSafeBeat Rx, Inc.2026-02-06
K252164NorthStar™ Mapping SystemImricor Medical Systems2026-01-28
K254085CARTO™ 3 EP Navigation System V9.0 with PIU PlusBiosense Webster, Inc.2026-01-18
K253733STAR Apollo™ Mapping SystemRhythm AI, Ltd.2025-12-19
K252533HemoSphere Alta Advanced Monitoring Platform (ALTAALL1; ALTACR1; ALTASR1)Edwards Lifesciences2025-12-18
K253141DeepRhythmAIMedicalgorithmics S.A.2025-12-11
K252238CoroFlow Cardiovascular SystemCoroventis Research AB2025-10-24
K252645LumiGuide Equipment R2.1; LumiGuide Wire; LumiGuide 3D HubPhilips Medical Systems Nederland B.V.2025-10-24