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Kolster Methods
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K935820
KOLSTER METHODS
July 19, 1994
K895761
GENERAL ASPERATOR
October 18, 1989
K895762
CANULA SUCTION FOR SURGICAL GENERAL AND PLASTIC
October 18, 1989