Product code
OYI: Non-bronchoscopic bronchoalveolar lavage catheter
FDA product code · Class I · Anesthesiology
Key facts
| Product code | OYI |
|---|---|
| Device | Non-bronchoscopic bronchoalveolar lavage catheter |
| Device class | Class I |
| Regulation number | 868.6810 |
| Review panel | Anesthesiology |
| Medical specialty | Anesthesiology |
| Submission type | 510(K) Exempt |
| GMP exempt | No |
| Implanted device | No |
| Life-sustaining or life-supporting | No |
| Definition | To perform non-bronchoscopic bronchoalveolar lavage (bal) in adult patients undergoing mechanical ventilation. |
At a glance
- 1–9 510(k) clearances
- None De Novo grants
- None PMA approvals
- None HDE approvals
- 10–99 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