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 Interferential Current Therapy
510(k) Number K883462
Device Name IF-II (TM), MODEL 9800
Applicant
MEDICAL DEVICES, INC.
833 THIRD ST. SOUTHWEST
ST. PAUL,  MN  55112
Applicant Contact A MACFARLANE
Correspondent
MEDICAL DEVICES, INC.
833 THIRD ST. SOUTHWEST
ST. PAUL,  MN  55112
Correspondent Contact A MACFARLANE
Regulation Number882.5890
Classification Product Code
LIH  
Date Received08/15/1988
Decision Date 05/24/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-