Clearance Summary
SYMBIOSIS ENT SURGICAL INSTRUMENTS received FDA 510(k) clearance under submission number K931793, sponsored by Symbiosis 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 1993-07-22.
- Submission: K931793
- Applicant / Sponsor: Symbiosis Corp.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class I
- Regulation citation: 21 CFR 874.4420
- Decision date: 1993-07-22
Classification & Regulation
This clearance is catalogued under FDA product code LRC and 21 CFR 874.4420, within the Ear, Nose, Throat review panel as a Class I device.