• 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 Media, Electroconductive
510(k) Number K022006
FOIA Releasable 510(k) K022006
Device Name CONDUCTIVE GEL
Applicant
THE DEZAC GROUP
719 A ST. NE
WASHINGTON,  DC  20002
Applicant Contact WENDY PARSLEY
Correspondent
THE DEZAC GROUP
719 A ST. NE
WASHINGTON,  DC  20002
Correspondent Contact WENDY PARSLEY
Regulation Number882.1275
Classification Product Code
GYB  
Date Received06/19/2002
Decision Date 09/13/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-