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 Table, Radiographic, Tilting
510(k) Number K912996
Device Name MODIF TOP DRIVE BOARD CXT-90 90/90 DIAG TILT TABLE
Applicant
Continental X-Ray Corp.
2000 S. 25th Ave.
Broadview,  IL  60153
Applicant Contact OCSAR KHUTORYANSKY
Correspondent
Continental X-Ray Corp.
2000 S. 25th Ave.
Broadview,  IL  60153
Correspondent Contact OCSAR KHUTORYANSKY
Regulation Number892.1980
Classification Product Code
IXR  
Date Received07/08/1991
Decision Date 02/03/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-