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 Massager, Therapeutic, Electric
510(k) Number K912634
Device Name CORDLESS ELECTRIC MASSAGER EV315
Applicant
Matsushita Electric Co.
1730 Pennsylvania Ave., NW
Washington,  DC  20006
Applicant Contact EDWARD M BASILE
Correspondent
Matsushita Electric Co.
1730 Pennsylvania Ave., NW
Washington,  DC  20006
Correspondent Contact EDWARD M BASILE
Regulation Number890.5660
Classification Product Code
ISA  
Date Received06/14/1991
Decision Date 09/12/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-