Product code QFD
- Device name
- Tens For Sinus Pain
- Medical specialty
- Neurology
- Device class
- 2
- Regulation number
- 882.5890
- Review panel
- NE
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Ineligible
- Definition
- Electrical stimulation to relieve pain
- Source
- FDA openFDA device classification dataset