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, double lumen for intestinal decompression and/or intubation
510(k) Number K971354
Device Name KNOTT NG TUBE
Applicant
MICHAEL M. KNOTT, M.D.
355 PINE ROSE CT.
TAHOE CITY,  CA  96145
Applicant Contact MICHAEL M KNOTT
Correspondent
MICHAEL M. KNOTT, M.D.
355 PINE ROSE CT.
TAHOE CITY,  CA  96145
Correspondent Contact MICHAEL M KNOTT
Regulation Number876.5980
Classification Product Code
FEG  
Date Received04/11/1997
Decision Date 11/19/1997
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
-
-