Clearance Summary
FRAZIER SUCTION TUBE received FDA 510(k) clearance under submission number K864382, sponsored by Luxtec 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 1987-01-14.
- Submission: K864382
- Applicant / Sponsor: Luxtec Corp.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class I
- Regulation citation: 21 CFR 874.4350
- Decision date: 1987-01-14
Classification & Regulation
This clearance is catalogued under FDA product code EQH and 21 CFR 874.4350, within the Ear, Nose, Throat review panel as a Class I device.