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Device, Monitoring, Intracranial Pressure

FDA product code GWM · 103 cleared devices

Class 2 Neurology
Regulation
21 CFR 882.1620
Review panel
NE
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1978-01-03 – 2026-04-10
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