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 K931732
Device Name VIFI: VECTOR INTERFERENTIAL ONE
Applicant
Compliance Technology, Inc.
3127 St. Johns Dr.
Murfreesboro,  TN  37129
Applicant Contact MICHAEL WILLY
Correspondent
Compliance Technology, Inc.
3127 St. Johns Dr.
Murfreesboro,  TN  37129
Correspondent Contact MICHAEL WILLY
Regulation Number882.5890
Classification Product Code
LIH  
Date Received04/07/1993
Decision Date 03/10/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-