Clearance Summary
MiiS Horus Bronchoscope; MiiS Horus Endoscope Display System -Tablet; MiiS Horus Endoscope Display System -Video Box received FDA 510(k) clearance under submission number K234113, sponsored by Medimaging Integrated Solution, Inc (Miis). 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 2024-05-01.
- Submission: K234113
- Applicant / Sponsor: Medimaging Integrated Solution, Inc (Miis)
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.4680
- Decision date: 2024-05-01
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.