Clearance Summary
ThermPix Thermovisual Camera received FDA 510(k) clearance under submission number K232462, sponsored by Usa Therm, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2023-09-14.
- Submission: K232462
- Applicant / Sponsor: Usa Therm, Inc.
- Clearance pathway: Special
- Review panel: Obstetrics/Gynecology
- Device class: Class I
- Regulation citation: 21 CFR 884.2980
- Decision date: 2023-09-14
Classification & Regulation
This clearance is catalogued under FDA product code LHQ and 21 CFR 884.2980, within the Obstetrics/Gynecology review panel as a Class I device.