FDA Product Code
FDA Product Code DTG — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Cardiovascular
- 21 CFR Citation
- 870.3690
510(k) Clearances — 5 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K092364 | MODEL 220 PATIENT MAGNET | Cyberonics, Inc. | 2009-11-03 | Traditional | PDF ↗ |
| K960849 | MAGNO ALARM | Cardiac Assist Devices, Inc. | 1997-03-26 | Traditional | PDF ↗ |
| K895110 | MAESTRO PACEMAKER TEST MAGNET | Cardiac Control Systems, Inc. | 1989-09-26 | Traditional | PDF ↗ |
| K831926 | IMPLANTABLE ENDOCARDIAL PACING LEADS | Oscor, Inc. | 1984-03-12 | Traditional | PDF ↗ |
| K813153 | TEST MAGNET | Pacesetter Systems | 1981-12-02 | Traditional | PDF ↗ |
Product code DTG · Class I · Cardiovascular. Data: openFDA.