Clearance Summary
ECHOSAMPLER received FDA 510(k) clearance under submission number K041237, sponsored by Gynetics Medical Products NV. 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 2004-09-08.
- Submission: K041237
- Applicant / Sponsor: Gynetics Medical Products NV
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.1060
- Decision date: 2004-09-08
Classification & Regulation
This clearance is catalogued under FDA product code HFF and 21 CFR 884.1060, within the Obstetrics/Gynecology review panel as a Class II device.