• 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 K905647
Device Name JENSEN III CHIROPRACTIC J-TABLE
Applicant
Freedman, Wolk and Co.
2530 Pennsylvania Ave. S.
St. Louis Park,  MN  55426
Applicant Contact FRANK B FREEDMAN
Correspondent
Freedman, Wolk and Co.
2530 Pennsylvania Ave. S.
St. Louis Park,  MN  55426
Correspondent Contact FRANK B FREEDMAN
Regulation Number890.3760
Classification Product Code
INQ  
Date Received12/17/1990
Decision Date 04/19/1991
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
-
-