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Sinusys Corporation
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K160770
Vent-Os Sinus Dilation family
June 29, 2016
K133016
VENT-OS SINUS DILATION SYSTEM
December 9, 2013