FDA Device Intelligence
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System, Telethermographic (Adjunctive Use)

FDA product code LHQ · Class 1 · Obstetrics/Gynecology

49
Registered devices
6
Adverse events
1
Recalls
41
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2017-01-14Med-Hot Thermal Imaging, Inc.Indications for use are not cleared or approved for market in the U.S.

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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.