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Airway Monitoring System

FDA product code OQU · 3 cleared devices

Class 2 Anesthesiology
Regulation
21 CFR 868.5730
Review panel
AN
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
2010-04-28 – 2020-05-15

The device is intended to assist in verifying ett tube placement, assist in detecting ett tube movement and obstruction of the tube tip

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