Product code
LXF: Diathermy, ultrasonic, for use other than applying therapeutic deep heat
FDA product code · Class III · Physical Medicine
Key facts
| Product code | LXF |
|---|---|
| Device | Diathermy, ultrasonic, for use other than applying therapeutic deep heat |
| Device class | Class III |
| Regulation number | 890.5300 |
| Review panel | Physical Medicine |
| Medical specialty | Physical Medicine |
| Submission type | PMA |
| GMP exempt | No |
| Implanted device | No |
| Life-sustaining or life-supporting | No |
At a glance
- None 510(k) clearances
- None De Novo grants
- None PMA approvals
- None HDE approvals
- None UDI devices (GUDID)
- 1–9 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