Product code FLJ
- Device name
- Unit, Airflow, Laminar
- Medical specialty
- General, Plastic Surgery
- Device class
- 2
- Regulation number
- 878.5070
- Review panel
- HO
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- Y
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset