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HMS — Drum, Eye Knife Test Class I

FDA Device Classification

Classification Details

Product Code: HMS
Device Class: Class I
Regulation Number: 886.4230
Submission Type
Review Panel: OP
Medical Specialty: Ophthalmic
Implant: No

Recent 510(k) Clearances

K-Number	Applicant	Device Name	Date
K926412	chiron vision	MICRON-SCOPE II	July 19, 1994