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Device, Positive Pressure Breathing, Intermittent

FDA product code NHJ · 23 cleared devices

Class 2 Anesthesiology
Regulation
21 CFR 868.5905
Review panel
AN
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1978-09-27 – 2026-08-24
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