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Msi

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K211178DURAMESH Mesh SutureSeptember 2, 2022
K960200INTROSTAT LEAD INTRODUCERJuly 2, 1996
K944226MSI PROCEDURE KITJune 21, 1995