• 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 Device, Iontophoresis, Other Uses
510(k) Number K041101
Device Name MEDICAL ADHESIVEONLINE, LLC. IONTOPHORESIS DRUG DELIVERY ELECTRODES, MODELS 23001, 23002, 23003, 23004, AND 24001
Applicant
MEDICAL ADHESIVEONLINE, LLC.
10809 GARDEN MIST
#2045
LAS VEGAS,  NV  89135
Applicant Contact ADAM SHAW
Correspondent
MEDICAL ADHESIVEONLINE, LLC.
10809 GARDEN MIST
#2045
LAS VEGAS,  NV  89135
Correspondent Contact ADAM SHAW
Regulation Number890.5525
Classification Product Code
EGJ  
Date Received04/26/2004
Decision Date 07/07/2004
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product Yes
-
-