K262735
- 510(k) number
- K262735
- Device name
- LINQ II Insertable Cardiac Monitor (ICM) (LNQ22)
- Applicant
- Medtronic, Inc. MN · US
- Product code
- MXD — Recorder, Event, Implantable Cardiac, (With Arrhythm
- Decision date
- 2026-08-28
- Date received
- 2026-07-31
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K262735.pdf
Official FDA record: K262735
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.