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Barosense, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K120126BAROSENSE ENDOGASTRIC TUBE AND INTRODUCER BOUGIESeptember 10, 2012
K120147ACE STAPLER AND CARTRIDGEFebruary 17, 2012
K110829ACE STAPLER AND CARTRIDGEJune 3, 2011
K082044ACE STAPLER, MODEL F0031May 11, 2010
K082589BAROSENSE ENDOGASTRIC TUBE (EGT), MODEL F0034May 22, 2009