• 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 K110071
Device Name COR ANALYZER
Applicant
Rcadia Medical Imaging , Ltd.
6 Sireni
Haifa,  IL 32972
Applicant Contact DAN LAOR
Correspondent
Rcadia Medical Imaging , Ltd.
6 Sireni
Haifa,  IL 32972
Correspondent Contact DAN LAOR
Regulation Number892.2050
Classification Product Code
LLZ  
Date Received01/10/2011
Decision Date 01/31/2011
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
-
-