Clearance Summary
GSI 37 AUTO TYMP received FDA 510(k) clearance under submission number K911095, sponsored by Lucas Grason-Stadler, Inc.. 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 1991-03-29.
- Submission: K911095
- Applicant / Sponsor: Lucas Grason-Stadler, Inc.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.1090
- Decision date: 1991-03-29
Classification & Regulation
This clearance is catalogued under FDA product code ETY and 21 CFR 874.1090, within the Ear, Nose, Throat review panel as a Class II device.