FDA 510(k)

LINQ II Insertable Cardiac Monitor (LNQ22)

K-Number: K233320 · 2023-10-31

Decision Date2023-10-31

Product CodeMXD

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

LINQ II Insertable Cardiac Monitor (LNQ22) is a medical device manufactured by Medtronic, Inc.. It received FDA 510(k) clearance on 2023-10-31 under approval number K233320. The device is classified under product code MXD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LINQ II Insertable Cardiac Monitor (LNQ22)?

LINQ II Insertable Cardiac Monitor (LNQ22) is a medical device that received FDA 510(k) clearance on 2023-10-31. It is manufactured by Medtronic, Inc.. The 510(k) number is K233320.

When was LINQ II Insertable Cardiac Monitor (LNQ22) approved by the FDA?

LINQ II Insertable Cardiac Monitor (LNQ22) received FDA 510(k) clearance on 2023-10-31, under approval number K233320.

What company makes LINQ II Insertable Cardiac Monitor (LNQ22)?

LINQ II Insertable Cardiac Monitor (LNQ22) is manufactured by Medtronic, Inc..

What is the FDA product code for LINQ II Insertable Cardiac Monitor (LNQ22)?

The FDA product code for LINQ II Insertable Cardiac Monitor (LNQ22) is MXD.

Related Clinical Trials

NCT06232876 Continuous Versus Intermittent Ward Monitoring NOT_YET_RECRUITING NCT01621594 Evaluating New Radiation Techniques for Cardiovascular Imaging RECRUITING NCT06172699 Assert-IQ Implantable Cardiac Monitor (ICM) Post Market Study COMPLETED NCT07405333 Effect of Coughing Exercises Versus Incentive Spirometry on Respiratory Function and Recovery in Children After Cardiac Surgery. RECRUITING NCT06589700 B2AD-Risk AFDAS Evolution of Burden of AF RECRUITING NCT03505801 Confirm Rx Insertable Cardiac Monitor SMART Registry COMPLETED

Other Devices by Medtronic, Inc.

K162896Affinity NT Oxygenator, Affinity NT Oxygenator with Trillium Biosurface K162892Achieve Advance Mapping Catheter K162054Medtronic Temporary External Pacemaker 53401 K162550Medtronic Model 5392 External Pulse Generator (EPG) K162016Affinity NT Oxygenator with Cortiva BioActive Surface K160983Kyphon HV-R Bone Cement

View all 137 devices →

Related Devices (Code: MXD)

K160809Reveal LINQMedtronic, Inc. K160689Reveal LINQMedtronic, Inc. K152995BioMonitor 2-AF, BioMonitor 2-SBiotronik, Inc. K171514BioMonitor 2-AF, BioMonitor 2-S, FIT - Fast Insert Tool 1 + 2, SetBiotronik, Inc. K170628BioMonitor 2-AF, BioMonitor 2-SBiotronik, Inc. K162855Reveal LINQMedtronic, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.