Clearance Summary
MARK I THERMAL IMAGER received FDA 510(k) clearance under submission number K023925, sponsored by Ix-Dr, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2003-02-11.
- Submission: K023925
- Applicant / Sponsor: Ix-Dr, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class I
- Regulation citation: 21 CFR 884.2980
- Decision date: 2003-02-11
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.