Product code MZM
- Device name
- Fibrin Sealant Preparation Device
- Medical specialty
- General Hospital
- Device class
- 2
- Regulation number
- 880.5860
- Review panel
- HE
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset