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Monitor, Carbon-Dioxide, Cutaneous

FDA product code LKD · 16 cleared devices

Class 2 Anesthesiology
Regulation
21 CFR 868.2480
Review panel
AN
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1988-12-16 – 2024-05-17
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