Clearance Summary
FirstSense Breast Exam received FDA 510(k) clearance under submission number K160573, sponsored by First Sense Medical, LLC. 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 2016-06-01.
- Submission: K160573
- Applicant / Sponsor: First Sense Medical, LLC
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class I
- Regulation citation: 21 CFR 884.2980
- Decision date: 2016-06-01
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.