ClearanceBrief
Company ยท US

Endoscopic Technologies, Inc. D/B/A Estech

FDA 510(k) clearances and medical device recalls filed under this name, 2009 to 2012. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
OCLSurgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue2
DWFCatheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass1
GCJLaparoscope, General & Plastic Surgery1
GEIElectrosurgical, Cutting & Coagulation & Accessories1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 20, 2012K113475ESTECH COBRA ADHERE XL 2 SURGICAL SYSTEM
Endoscopic Technologies, Inc. D/B/A Estech
OCL
Sep 23, 2011K110913ESTECH COBRA SURGICAL SYSTEM WITH THERMASHIELD ACCESSORY
Endoscopic Technologies, Inc. D/B/A Estech
OCL
Apr 7, 2010K100224ESTECH COBRA BIPOLSR II
Endoscopic Technologies, Inc. D/B/A Estech
GEI
Oct 20, 2009K091542ESTECH EASYFLOW CANNULA WITH GUIDEWIRE
Endoscopic Technologies, Inc. D/B/A Estech
DWF
Sep 15, 2009K091350ESTECH HAWKEYE INTRODUCER SYSTEMS
Endoscopic Technologies, Inc. D/B/A Estech
GCJ

Latest recalls

DateFirm and productCodeLinked 510(k)
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