• 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 supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
DeviceVIRAPAP HUMAN PAPILLOMAVIRUS DNA DETECTION KIT
Classification Namekit, dna detection, human papillomavirus
Generic Namekit, dna detection, human papillomavirus
Applicant
QIAGEN, INC.
1201 clopper road
gaithersburg, MD 20878
PMA NumberP880009
Supplement NumberS003
Date Received09/18/1989
Decision Date02/01/1990
Product Code
MAQ[ Registered Establishments with MAQ ]
Advisory Committee Microbiology
Supplement Typenormal 180 day track
Supplement Reason labeling change - indications/instructions/shelf life/tradename
Expedited Review Granted? No
Combination Product No
-
-