Clearance Summary
OMEGA OTO NASOPHARYNGO-LARYNGOSCOPE received FDA 510(k) clearance under submission number K920439, sponsored by Omega Universal Technologies, 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 1992-09-04.
- Submission: K920439
- Applicant / Sponsor: Omega Universal Technologies, Ltd.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.4760
- Decision date: 1992-09-04
Classification & Regulation
This clearance is catalogued under FDA product code EOB and 21 CFR 874.4760, within the Ear, Nose, Throat review panel as a Class II device.