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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: this medical device has supplements. The device description may have changed. Be sure to look at the supplements to get an up-to-date view of this device.
 
Trade NameVIRAPAP HUMAN PAPILLOMAVIRUS DNA DETECTION KIT
Classification Namekit, dna detection, human papillomavirus
Generic Namehuman papillomavirus dna detection kit
ApplicantQIAGEN, INC.
PMA NumberP880009
Date Received02/17/1988
Decision Date12/23/1988
Withdrawal Date 01/29/2010
Product Code
MAQ[ Registered Establishments with MAQ ]
Docket Number 88M-0446
Notice Date 02/28/1989
Advisory Committee Microbiology
Expedited Review Granted? No
Combination Product No
Supplements: S001 S002 S003 S004 S005 
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