Clearance Summary
NASOPHARYNGOSCOPE received FDA 510(k) clearance under submission number K934422, sponsored by Marks & Murase. 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 1994-01-27.
- Submission: K934422
- Applicant / Sponsor: Marks & Murase
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.4760
- Decision date: 1994-01-27
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.