Magnet, Test, Pacemaker
FDA product code DTG · Class I (low risk) · 21 CFR 870.3690 · Cardiovascular
5510(k) clearances
0PMA approvals
0recalls
Manufacturers
510(k) clearances
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K092364 | Model 220 Patient MagnetDTG · Traditional | Cyberonics, Inc. | 11/03/2009SE |
| K960849 | Magno AlarmDTG · Traditional | Cardiac Assist Devices, Inc. | 03/26/1997SE |
| K895110 | Maestro Pacemaker Test MagnetDTG · Traditional | Cardiac Control Systems, Inc. | 09/26/1989SE |
| K831926 | Implantable Endocardial Pacing LeadsDTG · Traditional | Oscor, Inc. | 03/12/1984SE |
| K813153 | Test MagnetDTG · Traditional | Pacesetter Systems | 12/02/1981SE |