LPO — Gases Used Within Eye To Place Pressure On Detached Retina Class III

FDA Device Classification

FDA product code LPO covers "Gases Used Within Eye To Place Pressure On Detached Retina", a Class III medical device regulated under 21 CFR 886.4270. Submissions are reviewed by the Ophthalmic panel.

Classification Details

Product Code
LPO
Device Class
Class III
Regulation Number
886.4270
Submission Type
Review Panel
OP
Medical Specialty
Ophthalmic
Implant
No