510(k) K251344

Device
OptiMap™ System
Applicant
Boston Scientific Corporation
510(k) number
K251344
Product code
DQK
Decision
Substantially Equivalent (SESE)
Decision date
2025-05-28
Date received
2025-04-30
Regulation
870.1425
Classification name
Computer, Diagnostic, Programmable
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Derek Charchuk
Address
4100 Hamline Ave. N St Paul MN US 55112 55112

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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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
K252429Vektor Computational ECG Mapping System (vMap®)Vektor Medical, Inc.2025-12-04
K252238CoroFlow Cardiovascular SystemCoroventis Research AB2025-10-24