MFK — Lens, Multifocal Intraocular Class III
FDA product code MFK covers "Lens, Multifocal Intraocular", a Class III medical device regulated under 21 CFR 886.3600. Submissions are reviewed by the Ophthalmic panel. Devices under this code are implants.
Classification Details
- Product Code
- MFK
- Device Class
- Class III
- Regulation Number
- 886.3600
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- Yes