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FDA 510(k), K200761, Tenax Laser Resistant Endotracheal Tube
FDA 510(k), K200761, Tenax Laser Resistant Endotracheal Tube
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$149.00 USD
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510(K) Number: K200761
Device Name: Tenax Laser Resistant Endotracheal Tube
Manufacturer: Bryan Medical, Inc.
Device Classification Name: Tube, Tracheal (W/Wo Connector)
Regulation Number: 868.5730
Classification Product Code: BTR
Date Received: 03/24/2020
Decision Date: 11/25/2020
Regulation Medical Specialty: Anesthesiology
Device Name: Tenax Laser Resistant Endotracheal Tube
Manufacturer: Bryan Medical, Inc.
Device Classification Name: Tube, Tracheal (W/Wo Connector)
Regulation Number: 868.5730
Classification Product Code: BTR
Date Received: 03/24/2020
Decision Date: 11/25/2020
Regulation Medical Specialty: Anesthesiology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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