Clearance Summary
Broncho Videoscope System received FDA 510(k) clearance under submission number K231521, sponsored by Scivita Medical Technology Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2023-11-14.
- Submission: K231521
- Applicant / Sponsor: Scivita Medical Technology Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.4680
- Decision date: 2023-11-14
Classification & Regulation
This clearance is catalogued under FDA product code EOQ and 21 CFR 874.4680, within the Ear, Nose, Throat review panel as a Class II device.