Sinusys Corporation

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K160770Vent-Os Sinus Dilation familyJune 29, 2016
K133016VENT-OS SINUS DILATION SYSTEMDecember 9, 2013