Product code
PMQ: Peripheral blood processing device for wound management
FDA product code · Class II · Hematology
Key facts
| Product code | PMQ |
|---|---|
| Device | Peripheral blood processing device for wound management |
| Device class | Class II |
| Regulation number | 864.9245 |
| Review panel | Hematology |
| Medical specialty | Hematology |
| Submission type | 510(k) |
| GMP exempt | No |
| Implanted device | No |
| Life-sustaining or life-supporting | No |
| Definition | Preparation of autologous platelet rich plasma gel from a small sample of peripheral blood for wound management. |
At a glance
- 10–99 510(k) clearances
- None De Novo grants
- None PMA approvals
- None HDE approvals
- 10–99 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