• 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 Test System, Antineutrophil Cytoplasmic Antibodies (Anca)
510(k) Number K974478
Device Name IMMUNO CONCEPTS ANCA TEST SYSTEMS
Applicant
Immuno Concepts, Inc.
2280 Springlake Rd.
Suite 106
Dallas,  TX  75234
Applicant Contact ERIC S HOY
Correspondent
Immuno Concepts, Inc.
2280 Springlake Rd.
Suite 106
Dallas,  TX  75234
Correspondent Contact ERIC S HOY
Regulation Number866.5660
Classification Product Code
MOB  
Date Received11/26/1997
Decision Date 02/09/1998
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Immunology
510k Review Panel Immunology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-