• 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 System, Image Processing, Radiological
510(k) Number K082269
Device Name VISAGE PACS, VERSION 6.0/CS 3.1
Applicant
Visage Imaging, Inc.
Lepsiusstrasse 70
Berlin,  DE 12163
Applicant Contact STEFAN STROWICH
Correspondent
Visage Imaging, Inc.
Lepsiusstrasse 70
Berlin,  DE 12163
Correspondent Contact STEFAN STROWICH
Regulation Number892.2050
Classification Product Code
LLZ  
Date Received08/11/2008
Decision Date 12/12/2008
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-