Home › Device types › QXJ
Whole Room Microbial Reduction Device
FDA product code QXJ · Class 2 · General Hospital
2
Registered devices
1
Adverse events
1
Recalls
2
510(k) clearances
Devices with this code
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-03-18 | XENEX Disinfection Services Inc. | Blackout curtains are no longer recommended as a protective barrier against UV/Ozone exposure to a bystander standing in the same room, but on the other side of |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.