HOQ — Grid, Amsler Class I

FDA Device Classification

Classification Details

Product Code
HOQ
Device Class
Class I
Regulation Number
886.1330
Submission Type
Review Panel
OP
Medical Specialty
Ophthalmic
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K180895oculocare medicalAlleyeJune 27, 2018
K143211vital art and science incorporatedmyVision Track Model 005March 20, 2015
K121738vital art and science incorporatedMYVISIONTRACK(TM)February 22, 2013
K014044notal visionMASCULAR COMPUTERIZED PSYCHOPHYSICAL TEST (MCPT)March 4, 2002
K874252richmond productsKREDA DISCJanuary 27, 1988
K863429wheel checkersMODIFIED DEVICE FOR SELF EXAMINATION OF EYESJanuary 20, 1987
K843227danek medicalMACULAR FUNCTION ANALYZERJuly 22, 1985
K843702wheel checkersAPPARATUS & METHODS SELF-EXAM OF EYEJanuary 3, 1985