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Optatint, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K854442
UVASORB-400
February 19, 1986
K850909
RHODA-LUX LENS BLANKS
October 4, 1985