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 Densitometer, Bone
510(k) Number K031991
Device Name DXAVIEW SPINE AND HIP, MODEL QCT-3D PLUS
Applicant
Image Analysis, Inc.
1380 Burkesville St.
Columbia,  KY  42728
Applicant Contact BEN ARNOLD
Correspondent
Image Analysis, Inc.
1380 Burkesville St.
Columbia,  KY  42728
Correspondent Contact BEN ARNOLD
Regulation Number892.1170
Classification Product Code
KGI  
Date Received06/27/2003
Decision Date 07/30/2003
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-