• 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 Antibodies, Gliadin
510(k) Number K993086
Device Name AUTOSTAT II ANTI-GLIADIN IGA ELISA
Applicant
Cogent Diagnotics , Ltd.
Pentlands Science Park
Bush Loan, Penicuik
Midlothian, Scotland,  GB EH26 OPL
Applicant Contact DANIELLE M KNIGHT
Correspondent
Cogent Diagnotics , Ltd.
Pentlands Science Park
Bush Loan, Penicuik
Midlothian, Scotland,  GB EH26 OPL
Correspondent Contact DANIELLE M KNIGHT
Regulation Number866.5750
Classification Product Code
MST  
Date Received09/15/1999
Decision Date 11/12/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Immunology
510k Review Panel Immunology
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-