Product code KPK
- Device name
- Marker, Ostia, Aorto-Saphenous Vein
- Medical specialty
- General, Plastic Surgery
- Device class
- 2
- Regulation number
- 878.4650
- Review panel
- CV
- Implant
- Y
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset