• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Premarket Approval (PMA)

  • 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
Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceQUANTIFERON-TB GOLD IN-TUBE
Generic Nametest, immunity, cell mediated, mycobacterium tuberculosis
ApplicantQIAGEN
19300 germantown road
germantown, MD 20874
PMA NumberP010033
Supplement NumberS017
Date Received08/30/2010
Decision Date05/26/2011
Product Code NCD 
Advisory Committee Microbiology
Supplement Typespecial (immediate track)
Supplement Reason labeling change - indications/instructions/shelf life/tradename
Expedited Review Granted? No
Combination ProductNo
Approval Order Statement  
APPROVAL FOR REVISIONS TO THE DEVICE PACKAGE INSERT AND MARKETING BOOKLET SUBSEQUENT TO THE PUBLICATION OFTHE CDC'S UPDATED GUIDELINES FOR USING INTERFERON GAMMA RELEASE ASSAYS TO DETECT MYCOBACTERIUM TUBERCULOSIS INFECTION - UNITED STATES, 2010, IN ACCORDANCE WITH THE ORIGINAL PMA POST-APPROVAL REQUIREMENT.
-
-