• 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 Nadh Oxidation/Nad Reduction, Ast/Sgot
510(k) Number K923505
Device Name AST (GOT) - ASPARTATE AMINOTRANSFERASE
Applicant
Randox Laboratories, Ltd.
Ardmore, Diamond Rd.
Crumlin, Bt29 4qy Co.
Antrim, N. Ireland,  IR
Applicant Contact John Lamont
Correspondent
Randox Laboratories, Ltd.
Ardmore, Diamond Rd.
Crumlin, Bt29 4qy Co.
Antrim, N. Ireland,  IR
Correspondent Contact John Lamont
Regulation Number862.1100
Classification Product Code
CIT  
Date Received07/15/1992
Decision Date 11/16/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-