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HKG — Fornixscope Class I

FDA Device Classification

FDA product code HKG covers "Fornixscope", a Class I medical device regulated under 21 CFR 886.1320. Submissions are reviewed by the Ophthalmic panel.

Classification Details

Product Code: HKG
Device Class: Class I
Regulation Number: 886.1320
Submission Type
Review Panel: OP
Medical Specialty: Ophthalmic
Implant: No