Home › Device types › KXN
Monitor, Cardiac, Fetal
FDA product code KXN · Class 2 · Obstetrics/Gynecology
0
Registered devices
21
Adverse events
1
Recalls
2
510(k) clearances
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2004-09-17 | Applied Medical Resources Corp | Inadequate trocar tip assembly that might yeild parts to patients. |
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.