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, Nuclear Magnetic Resonance Imaging
510(k) Number K121997
Device Name IMRIS ONCOLOGY PACKAGE
Applicant
Imris, Inc.
100-1370 Sony Pl.
Winnipeg, Mb,  CA R3T 1N5
Applicant Contact Sanjay Shah
Correspondent
Imris, Inc.
100-1370 Sony Pl.
Winnipeg, Mb,  CA R3T 1N5
Correspondent Contact Sanjay Shah
Regulation Number892.1000
Classification Product Code
LNH  
Subsequent Product Code
MOS  
Date Received07/09/2012
Decision Date 08/10/2012
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
-
-