Product code
PIA: Vibrator for climax control of premature ejaculation
FDA product code · Class II · Gastroenterology/Urology
Key facts
| Product code | PIA |
|---|---|
| Device | Vibrator for climax control of premature ejaculation |
| Device class | Class II |
| Regulation number | 876.5025 |
| Review panel | Gastroenterology/Urology |
| Medical specialty | Gastroenterology/Urology |
| Submission type | 510(K) Exempt |
| GMP exempt | No |
| Implanted device | No |
| Life-sustaining or life-supporting | No |
| Definition | Vibrator for climax control training for the treatment of premature ejaculation. |
At a glance
- None 510(k) clearances
- 1–9 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