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Humidifier, Respiratory Gas, (Direct Patient Interface)

FDA product code BTT · 214 cleared devices

Class 2 Anesthesiology
Regulation
21 CFR 868.5450
Review panel
AN
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1976-07-16 – 2026-08-27
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