Product code HOW
- Device name
- Drum, Opticokinetic
- Medical specialty
- Ophthalmic
- Device class
- 1
- Regulation number
- 886.1200
- Review panel
- OP
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- Y
- Third party review
- N
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset