510(k) clearance
LINQ II Insertable Cardiac Monitor (ICM) (LNQ22)
- 510(k) number
- K262735
- Applicant
- Medtronic, Inc.
- Decision date
- Aug 28, 2026
- Date received
- Jul 31, 2026
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Product code
- MXD
- Device type
- Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)
- Device class
- Class II
- Regulation
- 21 CFR 870.1025
- Advisory committee
- Cardiovascular
- Statement or summary
- Summary
- Third party
- N
- Location
- Mounds View, MN, US