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, Digital Image Communications, Radiological
510(k) Number K924229
Device Name VG-A MIG
Applicant
VORTECH DATA, INC.
2929 NORTH CENTRAL EXPRESSWAY
SUITE 101
RICHARDSON,  TX  75080
Applicant Contact KEM MYERS
Correspondent
VORTECH DATA, INC.
2929 NORTH CENTRAL EXPRESSWAY
SUITE 101
RICHARDSON,  TX  75080
Correspondent Contact KEM MYERS
Regulation Number892.2020
Classification Product Code
LMD  
Date Received08/21/1992
Decision Date 11/27/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-