Product code
RDW: General purpose laser products
FDA product code · Not Classified
Key facts
| Product code | RDW |
|---|---|
| Device | General purpose laser products |
| Device class | Not Classified |
| GMP exempt | Yes |
| Definition | Product, laser, general, emit beam; A laser or product containing a laser that is intended for general purpose use. |
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
- 1–9 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