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 Tubes, Gastrointestinal (And Accessories)
510(k) Number K112511
Device Name DOBBHOFF DUAL PORT FEEDING TUBE
Applicant
Covidien Lp, Formerly Registered AS Kendall
15 Hampshire St.
Mansfield,  MA  02048
Applicant Contact DEBORA STAPLETON
Correspondent
Covidien Lp, Formerly Registered AS Kendall
15 Hampshire St.
Mansfield,  MA  02048
Correspondent Contact DEBORA STAPLETON
Regulation Number876.5980
Classification Product Code
KNT  
Date Received08/30/2011
Decision Date 05/11/2012
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
-
-