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Surgidev Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K850729
ACUFLO VOLUMETRIC CONTROLLED DELIVERY SYS 2000
April 9, 1985
K831829
KARICKHOFF FLYING CORPUSCLE VIEWER
October 19, 1983
K831975
LEADING EDGE OPHTHALMIC KNIFE
August 31, 1983
K830008
KARICKHOFF KERATOSCOPE
January 26, 1983