510(k) K233562

Device
LINQ II Insertable Cardiac Monitor
Applicant
Medtronic, Inc.
510(k) number
K233562
Product code
MXD
Decision
Substantially Equivalent (SESE)
Decision date
2023-12-06
Date received
2023-11-06
Regulation
870.1025
Classification name
Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)
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
Kerry Luyster
Address
8200 Coral Sea St. N.E Mounds View MN US 55112 55112

FDA Registration Numbers

Source Documents

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

Related GUDID Devices

Primary DIBrandCompanyPublished
00763000891091CareLink SmartSync™ LINQ II™ Platform ApplicationMEDTRONIC, INC.2024-04-25

Other 510(k) Records For Product Code MXD

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K212008Reveal LINQ Insertable Cardiac MonitorMedtronic, Inc.2021-07-22
K210484LINQ II Insertable Cardiac Monitor, Zelda AI ECG Classification SystemMedtronic, Inc.2021-06-11
K211304LINQ II Insertable Cardiac MonitorMedtronic, Inc.2021-05-28