HOF
1989-01-31
Burr, Corneal, Manual
FDA product code HOF · 1 cleared devices
Class 1
Ophthalmic
- Regulation
- 21 CFR 886.4350
- Review panel
- OP
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1989-01-31 – 1989-01-31
No matching devices.
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