Home › Device types › LQK
Home Uterine Activity Monitor
FDA product code LQK · Class 2 · Obstetrics/Gynecology
1
Registered devices
0
Adverse events
1
Recalls
5
510(k) clearances
Devices with this code
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2016-08-04 | AirStrip Technologies, Inc. | Belt clip may become detached causing electronic components to be exposed. |
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.