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HOO — Perimeter, Ac-Powered Class I

FDA Device Classification

Classification Details

Product Code
HOO
Device Class
Class I
Regulation Number
886.1605
Submission Type
Review Panel
OP
Medical Specialty
Ophthalmic
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K941723welch allynWELCH ALLYN GLAUCOMA DETECTORJune 6, 1994
K930448marco ophthalmicMARCO PROJECTION PERIMETERJune 21, 1993
K873912richmond productsRICHMOND VISUAL FIELD SCREENERNovember 2, 1987
K864467keeler instrumentsHENSON - HAMBLIN CFS 2000 CENTRAL FIELD SCREENDecember 15, 1986
K860115bio-radDIGILAB CAMBRIDGE PERIMETERFebruary 27, 1986
K832800coopervisionAUTOMATIC TANGENT SCREEN 50September 29, 1983