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HLH — Pupillometer, Manual Class I

FDA Device Classification

Classification Details

Product Code
HLH
Device Class
Class I
Regulation Number
886.1700
Submission Type
Review Panel
OP
Medical Specialty
Ophthalmic
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K821083medical equipment designsP.D. METERJune 14, 1982
K821082medical equipment designsTRIAL LENS SETJune 14, 1982