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FDA 510(k) Applications Submitted by BAROSENSE, INC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K082044
07/18/2008
ACE STAPLER, MODEL F0031
BAROSENSE, INC
K082589
09/08/2008
BAROSENSE ENDOGASTRIC TUBE (EGT), MODEL F0034
BAROSENSE, INC
K120147
01/18/2012
ACE STAPLER AND CARTRIDGE
BAROSENSE, INC
K110829
03/24/2011
ACE STAPLER AND CARTRIDGE
BAROSENSE, INC
K120126
01/17/2012
BAROSENSE ENDOGASTRIC TUBE AND INTRODUCER BOUGIE
BAROSENSE, INC
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