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Optek Medico Co., Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K863048
OPM SLIT LAMP MODEL P-1 & MODEL P-3
September 3, 1986
K861854
OPM SLIT LAMP MODEL P-1
July 11, 1986
K843095
TRIA LENS SET
October 5, 1984