Product code GZN
- Device name
- Rheoencephalograph
- Medical specialty
- Neurology
- Device class
- 3
- Regulation number
- 882.1825
- Review panel
- NE
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Ineligible
- Definition
- Call for PMAs to be filed by 12/26/96 per 61 FR 50708 on 9/27/96
- Source
- FDA openFDA device classification dataset