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Port & Catheter, Implanted, Subcutaneous, Intraventricular

FDA product code LKG · 8 cleared devices

Class 2 Neurology
Regulation
21 CFR 882.5550
Review panel
HO
Implant
Yes
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1983-04-28 – 1995-05-09
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