• 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, X-Ray, Tomography, Computed
510(k) Number K123576
Device Name IMR SOFTWARE APPLICATION
Applicant
Philips Healthcare (Cleveland)
595 Miner Rd.
Cleveland,  OH  44143
Applicant Contact CHRISTINE ANDERSON
Correspondent
Philips Healthcare (Cleveland)
595 Miner Rd.
Cleveland,  OH  44143
Correspondent Contact CHRISTINE ANDERSON
Regulation Number892.1750
Classification Product Code
JAK  
Date Received11/20/2012
Decision Date 06/07/2013
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
-
-