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Optimed, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K903462
OPTIMED GLAUCOMA PRESSURE REGULATOR
October 16, 1990
K890687
ECT-100 ELECTRONIC CORNEAL TOPOGRAPHER
September 5, 1989
K884867
OPTIFIELD I AND II AUTOMATED PERIMETERS
March 9, 1989
K883458
OPTIMED ADVANTAGE
November 7, 1988