Product code HDO
- Device name
- Valve, Tubal Occlusion
- Medical specialty
- Obstetrics/Gynecology
- Device class
- 3
- Regulation number
- 884.5380
- Review panel
- OB
- Implant
- Y
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Ineligible
- Definition
- Call for PMAs 12/30/87 (52 FR 36883 10/1/87))
- Source
- FDA openFDA device classification dataset