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Cranial Electrotherapy Stimulator To Treat Insomnia And/Or Anxiety

FDA product code QJQ · Class 2 · Neurology

11
Registered devices
39
Adverse events
1
Recalls
19
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2023-04-06Fisher Wallace Laboratories Inc.If the batteries are installed incorrectly, the product may overheat, possibly leading to pain, discomfort, irritation, or even burns during use of the device.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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