Clearance Summary
AED HYSTEROSCOPE AND ACCESSORIES received FDA 510(k) clearance under submission number K141515, sponsored by National Advanced Endoscopy Devices, 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 2015-01-07.
- Submission: K141515
- Applicant / Sponsor: National Advanced Endoscopy Devices, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.1690
- Decision date: 2015-01-07
Classification & Regulation
This clearance is catalogued under FDA product code HIH and 21 CFR 884.1690, within the Obstetrics/Gynecology review panel as a Class II device.