• 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 Stimulator, Nerve, Transcutaneous, For Pain Relief
510(k) Number K843822
Device Name MEA110
Applicant
CANADIAN MEDICAL PRODUCTS
18 KENSINGTON ROAD
SUITE 203
BRAMALEA ONTARIO,  CA
Applicant Contact ALAN L RUSSELL
Correspondent
CANADIAN MEDICAL PRODUCTS
18 KENSINGTON ROAD
SUITE 203
BRAMALEA ONTARIO,  CA
Correspondent Contact ALAN L RUSSELL
Regulation Number882.5890
Classification Product Code
GZJ  
Date Received09/28/1984
Decision Date 10/22/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-