K233562
- 510(k) number
- K233562
- Device name
- LINQ II Insertable Cardiac Monitor
- Applicant
- Medtronic, Inc. MN · US
- Product code
- MXD — Recorder, Event, Implantable Cardiac, (With Arrhythm
- Decision date
- 2023-12-06
- Date received
- 2023-11-06
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K233562.pdf
Official FDA record: K233562
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.