Product code KZA
- Device name
- Device, Vein Location, Liquid Crystal
- Medical specialty
- General Hospital
- Device class
- 1
- Regulation number
- 880.6970
- Review panel
- HO
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset