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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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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 NumberS001
Date Received04/04/1989
Decision Date06/06/1989
Product Code
MAQ[ Registered Establishments with MAQ ]
Advisory Committee Microbiology
Supplement Typenormal 180 day track
Supplement Reason location change - manufacturer/sterilizer/packager/supplier
Expedited Review Granted? No
Combination Product No
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