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 Solid State X-Ray Imager (Flat Panel/Digital Imager)
510(k) Number K172784
Device Name DX-D Imaging Package
Applicant
Agfa HealthCare N.V.
Septestraat 27
Mortsel,  BE B-2640
Applicant Contact Wim Govaerts
Correspondent
Agfa Healthcare
10 South Academy Street
Greenville,  SC  29601
Correspondent Contact ShaeAnn Cavanagh
Regulation Number892.1680
Classification Product Code
MQB  
Date Received09/15/2017
Decision Date 10/13/2017
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-