• 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 Stretcher, Wheeled, Powered
510(k) Number K844711
Device Name MODELS 134, 135 & 136 TRANSFER CART/TABLE
Applicant
Tri W-G, Inc.
P.O. Box 905
Valley City,  ND  58072
Applicant Contact FRANK H ERLING
Correspondent
Tri W-G, Inc.
P.O. Box 905
Valley City,  ND  58072
Correspondent Contact FRANK H ERLING
Regulation Number890.3690
Classification Product Code
INK  
Date Received12/03/1984
Decision Date 03/05/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-