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 tube, feeding
510(k) Number K892431
Device Name KENDALL CURITY FEEDING TUBES
Applicant
THE KENDAL CO.
ONE FEDERAL ST.
BOSTON,  MA  02110 -2003
Applicant Contact WILLIAM D CURTIN
Correspondent
THE KENDAL CO.
ONE FEDERAL ST.
BOSTON,  MA  02110 -2003
Correspondent Contact WILLIAM D CURTIN
Regulation Number876.5980
Classification Product Code
FPD  
Date Received04/10/1989
Decision Date 05/19/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-