Clearance Summary
Tenax® Laser Resistant Endotracheal Tube received FDA 510(k) clearance under submission number K251794, sponsored by Bryan Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2026-09-03.
- Submission: K251794
- Applicant / Sponsor: Bryan Medical, Inc.
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5730
- Decision date: 2026-09-03
Classification & Regulation
This clearance is catalogued under FDA product code BTR and 21 CFR 868.5730, within the Anesthesiology review panel as a Class II device.