• 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 Assembly, Tube Housing, X-Ray, Diagnostic
510(k) Number K933162
Device Name MRX-750
Applicant
Mrx Corp.
320 Westway Pl.
Suite 520
Arlington,  TX  76018
Applicant Contact DON DARROW
Correspondent
Mrx Corp.
320 Westway Pl.
Suite 520
Arlington,  TX  76018
Correspondent Contact DON DARROW
Regulation Number892.1760
Classification Product Code
ITY  
Date Received06/29/1993
Decision Date 10/07/1993
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
-
-