HNE — Snare, Enucleating Class I

FDA Device Classification

FDA product code HNE covers "Snare, Enucleating", a Class I medical device regulated under 21 CFR 886.4350. Submissions are reviewed by the Ophthalmic panel.

Classification Details

Product Code
HNE
Device Class
Class I
Regulation Number
886.4350
Submission Type
Review Panel
OP
Medical Specialty
Ophthalmic
Implant
No