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HOS — Projector, Ophthalmic Class I

FDA Device Classification

Classification Details

Product Code
HOS
Device Class
Class I
Regulation Number
886.1680
Submission Type
Review Panel
OP
Medical Specialty
Ophthalmic
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K936200canon usaWIRELESS CHART PROJECTOR,HCP-W 721September 28, 1994
K930443marco ophthalmicMARCO CP-600 AUTO CHART PROJECTOR/CP-1 CHART PROJEJuly 6, 1993
K924784r.h. burtonBURTON PROJECTOR HEAD - MODEL 6000-HApril 5, 1993
K921214luneau ophtalmologieOPHTHALMIC PROJECTORJune 11, 1992
K890992woodlynWOODLYN OPHTHALMIC PROJECTORMay 17, 1989
K862519bausch and lombBAUSCH & LOMB ACCU-CHART 3 ACUITY PROJECTORJuly 23, 1986
K812706mosebach electric and supplyMILLER/NADLER GLARE TESTERNovember 16, 1981
K811180american opticalULTRAMATIC PROJECT-O-CHART OPHTH. PROJMay 15, 1981
K781658bausch and lombPROJECTOR, ACCU-CHART ACUITYOctober 17, 1978