• 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 sleeve, limb, compressible
510(k) Number K841235
Device Name MEDO MEDOMER MBF-100 II
Applicant
MEDO U.S.A., INC.
P.O. BOX 129
WOOD DALE,  IL  60191
Applicant Contact HIROSHI OKAZAKI
Correspondent
MEDO U.S.A., INC.
P.O. BOX 129
WOOD DALE,  IL  60191
Correspondent Contact HIROSHI OKAZAKI
Regulation Number870.5800
Classification Product Code
JOW  
Date Received03/22/1984
Decision Date 11/19/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-