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 Stimulator, Muscle, Powered
510(k) Number K904332
Device Name MSTIM-2000 EMS
Applicant
Oms Medical Supplies, Inc.
230 Libbey Pkwy.
Weymouth,  MA  02189
Applicant Contact THOMAS RIIHIMAKI
Correspondent
Oms Medical Supplies, Inc.
230 Libbey Pkwy.
Weymouth,  MA  02189
Correspondent Contact THOMAS RIIHIMAKI
Regulation Number890.5850
Classification Product Code
IPF  
Date Received09/21/1990
Decision Date 05/01/1991
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
-
-