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Catheter, Percutaneous, Intraspinal, Short Term

FDA product code MAJ · 6 cleared devices

Class 2 Anesthesiology
Regulation
21 CFR 868.5120
Review panel
HO
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1989-11-01 – 1997-03-18
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