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Kis Products
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K984380
DISPO ETCH
August 6, 2001
K993182
DISPOPROPHY
August 6, 2001
K993124
DISPODRILL
August 6, 2001