Product code
QHC: Instrument, biopsy, core, soft tissue, female reproductive organs
FDA product code · Class II · Obstetrics/Gynecology
Key facts
| Product code | QHC |
|---|---|
| Device | Instrument, biopsy, core, soft tissue, female reproductive organs |
| Device class | Class II |
| Regulation number | 876.1075 |
| Review panel | Obstetrics/Gynecology |
| Medical specialty | Gastroenterology/Urology |
| Submission type | 510(k) |
| GMP exempt | No |
| Implanted device | No |
| Life-sustaining or life-supporting | No |
| Definition | Obtain core soft tissue biopsy samples of internal female reproductive organs such as uterus, ovaries, and retroperitoneal lymph nodes. |
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