DTG — Magnet, Test, Pacemaker Class I
FDA Device Classification
Classification Details
- Product Code
- DTG
- Device Class
- Class I
- Regulation Number
- 870.3690
- Submission Type
- Review Panel
- CV
- Medical Specialty
- Cardiovascular
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K092364 | cyberonics | MODEL 220 PATIENT MAGNET | November 3, 2009 |
| K960849 | cardiac assist devices | MAGNO ALARM | March 26, 1997 |
| K895110 | cardiac control systems | MAESTRO PACEMAKER TEST MAGNET | September 26, 1989 |
| K831926 | oscor | IMPLANTABLE ENDOCARDIAL PACING LEADS | March 12, 1984 |
| K813153 | pacesetter systems | TEST MAGNET | December 2, 1981 |