K233320
- 510(k) number
- K233320
- Device name
- LINQ II Insertable Cardiac Monitor (LNQ22)
- Applicant
- Medtronic, Inc. MN · US
- Product code
- MXD — Recorder, Event, Implantable Cardiac, (With Arrhythm
- Decision date
- 2023-10-31
- Date received
- 2023-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
510(k) Summary (official FDA PDF): K233320.pdf
Official FDA record: K233320
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.