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 K133096
Device Name ABB VIE J
Applicant
AbbVie , Inc.
1 N. Waukegan Rd.
North Chicago,  IL  60064
Applicant Contact KATHERINE WORTLEY
Correspondent
AbbVie , Inc.
1 N. Waukegan Rd.
North Chicago,  IL  60064
Correspondent Contact KATHERINE WORTLEY
Regulation Number876.5980
Classification Product Code
KNT  
Date Received09/30/2013
Decision Date 06/18/2014
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
-
-