Product code
HDO: Valve, tubal occlusion
FDA product code · Class III · Obstetrics/Gynecology
Key facts
| Product code | HDO |
|---|---|
| Device | Valve, tubal occlusion |
| Device class | Class III |
| Regulation number | 884.5380 |
| Review panel | Obstetrics/Gynecology |
| Medical specialty | Obstetrics/Gynecology |
| Submission type | PMA |
| GMP exempt | No |
| Implanted device | Yes |
| Life-sustaining or life-supporting | No |
| Definition | Call for PMAs 12/30/87 (52 FR 36883 10/1/87)) |
At a glance
- None 510(k) clearances
- None De Novo grants
- None PMA approvals
- None HDE approvals
- None UDI devices (GUDID)
- None MAUDE adverse event reports
- None Recalled products (Z-numbers)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device product codes
FDA product codes classify medical devices by type and intended use; each code maps to a device class, a classification regulation and a review panel.
Source: U.S. Food and Drug Administration (FDA), Product Classification database