Medtronic Inc., Cardiac Rhythm and Heart Failure
3 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| Medtronic, Viva Quadripolar Implantable Cardioverter Defibrillators: Product Model VIVAXTC recall (Z-2650-2016) | Medtronic Inc., Cardiac Rhythm and Heart Failure | 2016-08-25 |
| Medtronic, Evera Implantable Cardioverter Defibrillators: Product Model EVERA XT DDBB1D1, recall (Z-2651-2016) | Medtronic Inc., Cardiac Rhythm and Heart Failure | 2016-08-25 |
| Medtronic, MyCareLink Patient Monitor, Model 24950, Rx Only. The MyCareLink Monitor, Model recall (Z-2125-2016) | Medtronic Inc., Cardiac Rhythm and Heart Failure | 2016-07-05 |
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Every clearance here is in the API, with alerts when new ones post.