Product code KRF
- Device name
- Charger, Pacemaker
- Medical specialty
- Cardiovascular
- Device class
- 1
- Regulation number
- 870.3670
- Review panel
- CV
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset