• 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 Table, Physical Therapy, Multi Function
510(k) Number K922980
Device Name 745-M (MAGNUM)
Applicant
Tri W-G, Inc.
P.O. Box 905
Valley City,  ND  58072
Applicant Contact KAVID KESLER
Correspondent
Tri W-G, Inc.
P.O. Box 905
Valley City,  ND  58072
Correspondent Contact KAVID KESLER
Regulation Number890.5880
Classification Product Code
JFB  
Date Received06/22/1992
Decision Date 07/13/1992
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
-
-