Clearance Summary
RLS 9100 RHINO-LARYNGEAL STROBOSCOPE received FDA 510(k) clearance under submission number K921184, sponsored by Kay Elemetrics Corp.. 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 1992-05-28.
- Submission: K921184
- Applicant / Sponsor: Kay Elemetrics Corp.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class I
- Regulation citation: 21 CFR 874.4750
- Decision date: 1992-05-28
Classification & Regulation
This clearance is catalogued under FDA product code EQL and 21 CFR 874.4750, within the Ear, Nose, Throat review panel as a Class I device.