• 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 K041935
Device Name DR SYSTEMS PACS, RELEASE 6.1
Applicant
DR. SYSTEMS, INC.
10140 MESA RIM RD.
san diego,  CA  92121
Applicant Contact kimberly j meade
Correspondent
DR. SYSTEMS, INC.
10140 MESA RIM RD.
san diego,  CA  92121
Correspondent Contact kimberly j meade
Regulation Number892.2050
Classification Product Code
LLZ  
Date Received07/19/2004
Decision Date 08/16/2004
Decision substantially equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
summary summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-