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 System, X-Ray, Tomography, Computed
510(k) Number K191394
Device Name ILLUMISITE Platform
Applicant
Covidien, LLC
161 Cheshire Lane N, Suite 100
Plymouth,  MN  55441
Applicant Contact Kristi Fox
Correspondent
Covidien, LLC
161 Cheshire Lane N, Suite 100
Plymouth,  MN  55441
Correspondent Contact Kristi Fox
Regulation Number892.1750
Classification Product Code
JAK  
Date Received05/24/2019
Decision Date 08/07/2019
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
Recalls CDRH Recalls
-
-