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Monitor, Air Embolism, Ultrasonic

FDA product code CBA · 1 cleared devices

Class 2 Anesthesiology
Regulation
21 CFR 868.2025
Review panel
AN
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1978-07-17 – 1978-07-17
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