Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Electrosurgical, Cutting & Coagulation & Accessories
510(k) Number K133017
Device Name ESTECH COBRA(R) GENESIS BIPOLAR CLAMP
Applicant
Estech, Inc.
2603 Camino Ramon
Suite 100
San Ramon,  CA  94583
Applicant Contact TAMER IBRAHIM
Correspondent
Estech, Inc.
2603 Camino Ramon
Suite 100
San Ramon,  CA  94583
Correspondent Contact TAMER IBRAHIM
Regulation Number878.4400
Classification Product Code
GEI  
Date Received09/26/2013
Decision Date 10/07/2013
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-