Product code
QLH: System, intravaginal, for controlled release of drug substance, cder or cber led
FDA product code · Not Classified · Obstetrics/Gynecology
Key facts
| Product code | QLH |
|---|---|
| Device | System, intravaginal, for controlled release of drug substance, cder or cber led |
| Device class | Not Classified |
| Review panel | Obstetrics/Gynecology |
| Submission type | Contact ODE |
| GMP exempt | No |
| Implanted device | No |
| Life-sustaining or life-supporting | No |
| Definition | Intravaginal systems for controlled release of drug substance are products that are inserted into the vagina and provide controlled release of drug products |
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