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Endoscopic Technologies, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K060101ESTECH AORTIC EASY FLOW CANNULAMay 10, 2006
K053326ESTECH COBRA ELECTROSURGICAL UNIT & CABLEJanuary 6, 2006
K053100ESTECH COBRA BIPOLAR SYSTEMDecember 19, 2005
K946105ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIESApril 6, 1995
K945978TUBING, NONINVASIVEJanuary 11, 1995
K945979TROCAR/CANNULADecember 21, 1994
K924057DISPOSIBLE ELECTRO COAGULATION PROBEMarch 11, 1994
K922685TROCARSApril 5, 1993