Clearance Summary
Elvie Stride 2 received FDA 510(k) clearance under submission number K242125, sponsored by Chiaro Technology, Ltd.. 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 2024-09-27.
- Submission: K242125
- Applicant / Sponsor: Chiaro Technology, Ltd.
- Clearance pathway: Special
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.5160
- Decision date: 2024-09-27
Classification & Regulation
This clearance is catalogued under FDA product code HGX and 21 CFR 884.5160, within the Obstetrics/Gynecology review panel as a Class II device.