FDA Device Intelligence
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Alarm, Conditioned Response Enuresis

FDA product code KPN · Class 2 · Gastroenterology, Urology

145
Registered devices
965
Adverse events
4
Recalls
37
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2022-09-30Baxter Healthcare CorporationRadio frequency emission from a functioning WatchCare device may potentially impact other devices (including, but not limited to telemetry devices, bladder scan
2022-09-30Baxter Healthcare CorporationRadio frequency emission from a functioning WatchCare device may potentially impact other devices (including, but not limited to telemetry devices, bladder scan
2022-09-30Baxter Healthcare CorporationRadio frequency emission from a functioning WatchCare device may potentially impact other devices (including, but not limited to telemetry devices, bladder scan
2022-09-30Baxter Healthcare CorporationRadio frequency emission from a functioning WatchCare device may potentially impact other devices (including, but not limited to telemetry devices, bladder scan

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.