COMPANY
Bryan Corporation
Timeline
- FDA FDA 510(k) clearance: Tenax® Laser Resistant Endotracheal Tube — K251794, Sep 3, 2026. Applicant at approval: Bryan Medical, Inc. source ↗
FDA records (last 2 years)
- FDA 510(k) clearance: Tenax® Laser Resistant Endotracheal Tube — K251794, Sep 3, 2026. Applicant at approval: Bryan Medical, Inc. source ↗
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