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 Stents, Drains And Dilators For The Biliary Ducts
510(k) Number K251658
Device Name Endoflux™ Biliary & Pancreatic Stent Sets
Applicant
Medi-Globe GmbH
Medi-Globe St. 1-5
Achenmuehle,  DE 83101
Applicant Contact Stephan Schneider
Correspondent
Medi-Globe GmbH
Medi-Globe St. 1-5
Achenmuehle,  DE 83101
Correspondent Contact Stephan Schneider
Regulation Number876.5010
Classification Product Code
FGE  
Date Received05/30/2025
Decision Date 04/16/2026
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-