Medtronic, Inc. · Class II · Cleared Jul 3, 2020
| K-number | K200795 |
| Device name | LINQ II Insertable Cardiac Monitor, LINQ Mobile Manager, Device Command Library, Instrument Command Library, LINQ Tool Kit |
| Applicant | Medtronic, Inc. |
| Product code | MXD |
| Device class | Class II |
| Decision date | Jul 3, 2020 |
| Decision | Substantially Equivalent |
| Regulation | 870.1025 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov