Home / Device Classification / HPK

HPK — Tonograph Class II

FDA Device Classification

FDA product code HPK covers "Tonograph", a Class II medical device regulated under 21 CFR 886.1930. Submissions are reviewed by the Ophthalmic panel.

Classification Details

Product Code: HPK
Device Class: Class II
Regulation Number: 886.1930
Submission Type
Review Panel: OP
Medical Specialty: Ophthalmic
Implant: No