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 K020516
Device Name CARE IFC PLUS
Applicant
Care Rehab, Inc.
1124 Dominion Court
Mclean,  VA  22102
Applicant Contact CHRISTIAN E HUNT
Correspondent
Care Rehab, Inc.
1124 Dominion Court
Mclean,  VA  22102
Correspondent Contact CHRISTIAN E HUNT
Regulation Number882.5890
Classification Product Code
LIH  
Date Received02/15/2002
Decision Date 05/16/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-