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Stimulator, Nerve, Peripheral, Electric

FDA product code KOI · 29 cleared devices

Class 2 Anesthesiology
Regulation
21 CFR 868.2775
Review panel
AN
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1984-02-17 – 2026-05-22
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