DTG
5 FDA 510(k) clearances · Product code
90 daysmedian time to decision
400 days90th percentile
5clearances measured
FDA profile
- Official device name
- Magnet, Test, Pacemaker
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 870.3690
- Medical specialty
- Cardiovascular
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| MODEL 220 PATIENT MAGNET (K092364) | Cyberonics, Inc. | 2009-11-03 |
| MAGNO ALARM (K960849) | Cardiac Assist Devices, Inc. | 1997-03-26 |
| MAESTRO PACEMAKER TEST MAGNET (K895110) | Cardiac Control Systems, Inc. | 1989-09-26 |
| IMPLANTABLE ENDOCARDIAL PACING LEADS (K831926) | Oscor, Inc. | 1984-03-12 |
| TEST MAGNET (K813153) | Pacesetter Systems | 1981-12-02 |
Track DTG automatically
Every clearance here is in the API, with alerts when new ones post.