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HOK — Screen, Tangent, Projection, Ac-Powered Class I

FDA Device Classification

Classification Details

Product Code: HOK
Device Class: Class I
Regulation Number: 886.1810
Submission Type
Review Panel: OP
Medical Specialty: Ophthalmic
Implant: No

Recent 510(k) Clearances

K-Number	Applicant	Device Name	Date
K914896	clement clarke	FRIEDMANN ANALYSER 3	January 23, 1992