MJP — Lens, Intraocular, Toric Optics Class III

FDA Device Classification

FDA product code MJP covers "Lens, Intraocular, Toric Optics", 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
MJP
Device Class
Class III
Regulation Number
886.3600
Submission Type
Review Panel
OP
Medical Specialty
Ophthalmic
Implant
Yes