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Aegis Surgical, Ltd.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K160171Illuminated Mediastinal Access PortFebruary 26, 2016
K141622ILLUMINATED MEDIASTINOSCOPEJanuary 9, 2015