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Instrument, Shunt System Implantation

FDA product code GYK · 13 cleared devices

Class 1 Neurology
Regulation
21 CFR 882.4545
Review panel
NE
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1977-08-16 – 1996-10-11
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