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 K963186
Device Name ORTHO 8000
Applicant
Inner Vision Mri , Ltd.
719 Catalpa Ave.
Teaneck,  NJ  07666
Applicant Contact DIANA UPTON
Correspondent
Inner Vision Mri , Ltd.
719 Catalpa Ave.
Teaneck,  NJ  07666
Correspondent Contact DIANA UPTON
Regulation Number892.1000
Classification Product Code
LNH  
Date Received08/14/1996
Decision Date 11/12/1996
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
-
-