Barosense, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BAROSENSE ENDOGASTRIC TUBE AND INTRODUCER BOUGIE, ACE STAPLER AND CARTRIDGE, ACE STAPLER AND CARTRIDGE
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Barosense, Inc. Gastroenterology & Urology ✕
5 devices
Cleared
Sep 10, 2012
BAROSENSE ENDOGASTRIC TUBE AND INTRODUCER BOUGIE
Gastroenterology & Urology
237d
Cleared
Feb 17, 2012
ACE STAPLER AND CARTRIDGE
Gastroenterology & Urology
30d
Cleared
Jun 03, 2011
ACE STAPLER AND CARTRIDGE
Gastroenterology & Urology
71d
Cleared
May 11, 2010
ACE STAPLER, MODEL F0031
Gastroenterology & Urology
662d
Cleared
May 22, 2009
BAROSENSE ENDOGASTRIC TUBE (EGT), MODEL F0034
Gastroenterology & Urology
256d