Usgi Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K103688G-PROX EZ ENDOSCOPIC GRASPERJanuary 14, 2011
K102931G-CINCH SUTURE GRASPERDecember 30, 2010
K102916G-CATH TISSUE ANCHOR DELIVERY CATHETEROctober 20, 2010
K100251G-CATH TISSUE ANCHOR DELIVERY CATHETER, MODELS 205302, 205333February 17, 2010
K093018G-PROX ENDOSCOPIC GRASPER, MODEL 205333October 7, 2009
K072405USGI TRANSPORT ENDOSCOPIC ACCESS DEVICESeptember 13, 2007
K061276G-PROX ENDOSCOPIC GRASPERDecember 6, 2006
K061268G-LIX TISSUE GRASPERJuly 31, 2006
K061216USGI TRANSPORT ENDOSCOPIC GUIDEMay 15, 2006
K051919MODIFICATION TO: USGI SHAPELOCK ENDOSCOPIC GUIDEJuly 26, 2005
K050253USGI SHAPELOCK ENDOSCOPIC GUIDEFebruary 28, 2005
K033954SHAPE LOCKING ENDOSCOPIC OVERTUBEMarch 19, 2004
K023902SHAPE-LOCKABLE ENDOSCOPIC OVERTUBEAugust 20, 2003