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HOM — Screen, Tangent, Ac-Powered (Campimeter) Class I

FDA Device Classification

Classification Details

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

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K860642biosan laboratoriesPHOTRON VISUAL FIELD ANALYZERApril 15, 1986