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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