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Humidifier, Non-Direct Patient Interface (Home-Use)

FDA product code KFZ · 20 cleared devices

Class 1 Anesthesiology
Regulation
21 CFR 868.5460
Review panel
AN
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1976-08-11 – 1995-02-10
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