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 Radiological Image Processing Software For Radiation Therapy
510(k) Number K220598
Device Name AutoContour Model RADAC V2
Applicant
Radformation, Inc.
335 Madison Avenue, 4th floor
New York,  NY  10017
Applicant Contact Kurt Sysock
Correspondent
Radformation, Inc.
335 Madison Avenue, 4th floor
New York,  NY  10017
Correspondent Contact Kurt Sysock
Regulation Number892.2050
Classification Product Code
QKB  
Date Received03/02/2022
Decision Date 08/24/2022
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-