• 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 Orthosis, Truncal, For Dysmenorrhea
510(k) Number K003128
Device Name MODIFICATION TO RELIEF BRIEF
Applicant
THE JM KOHN CO.
201 SPEAR ST.
SUITE 1600
SAN FRANCISCO,  CA  94105 -1635
Applicant Contact CHARLES L MORIN
Correspondent
THE JM KOHN CO.
201 SPEAR ST.
SUITE 1600
SAN FRANCISCO,  CA  94105 -1635
Correspondent Contact CHARLES L MORIN
Regulation Number890.3490
Classification Product Code
NJB  
Date Received10/06/2000
Decision Date 08/12/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-