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 Table, Powered
510(k) Number K940131
Device Name TABLE MAT MORTORIZED/ELECTRIC
Applicant
Med Mart, Inc.
215 12th Ave. Northeast
P.O. Box 905
Valley City,  ND  58072
Applicant Contact DAVID KESLER
Correspondent
Med Mart, Inc.
215 12th Ave. Northeast
P.O. Box 905
Valley City,  ND  58072
Correspondent Contact DAVID KESLER
Regulation Number890.3760
Classification Product Code
INQ  
Subsequent Product Code
INW  
Date Received01/03/1994
Decision Date 02/25/1994
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
-
-