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/ Endophys, Inc.
Endophys, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K160272
Endophys Pressure Sensing Sheath Kit
March 4, 2016
K141275
ENDOPHYS PRESSURE SENSING SHEATH KIT
January 7, 2015
K141615
ENDOPHYS BLOOD PRESSURE MONITOR
January 7, 2015