GXE
1992-12-08
Leukotome
FDA product code GXE · 1 cleared devices
Class 1
Neurology
- Regulation
- 21 CFR 882.4600
- Review panel
- NE
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1992-12-08 – 1992-12-08
No matching devices.
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