Estech, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K133017ESTECH COBRA(R) GENESIS BIPOLAR CLAMPOctober 7, 2013
K053021ESTECH CLEARVIEW MV ATRIAL DEPRESSORJanuary 26, 2006
K052081REMOTE ACCESS PERFUSION (RAP) FEMORAL VENOUS CANNULADecember 16, 2005
K051749COBRA SURGICAL SYSTEMSeptember 13, 2005
K041599COBRA ADHERE SURGICAL SYSTEMJuly 27, 2004
K032632REMOTE ACCESS PERFUSION CANNULA LEFT AXILLARY 21 FRENCHOctober 22, 2003
K990573ESTECH ARTERIAL REMOTE ACCESS PERFUSION CANNULAMarch 11, 1999