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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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1 to 10 of 38 Results
PMA Number P890064 Decision Date To 07/07/2015
 
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VIRATYPE HUMAN PAPILLOMAVIRUS DNA TYPING KIT QIAGEN GAITHERSBURG, INC P890064 03/11/1991
VIRATYPE HUMAN PAPILLOMAVIRUS DNA TYPING KIT QIAGEN GAITHERSBURG, INC P890064 S001 05/17/1993
VIRATYPE HUMAN PAPILLOMAVIRUS DNA TYPING KIT QIAGEN GAITHERSBURG, INC P890064 S002 05/19/1994
HYBRID CAPTURE(TM) SYSTEM VIRATYPE(R) PLUS HPV DNA QIAGEN GAITHERSBURG, INC P890064 S003 04/28/1995
HYBRID CAPTURE(TM) SYSTEM HPV DNA ASSAY QIAGEN GAITHERSBURG, INC P890064 S004 08/28/1996
HYBRID CAPTURE(TM) SYSTEM HPV DNA ASSAY QIAGEN GAITHERSBURG, INC P890064 S005 08/15/1997
HCII HPV TEST (DIGENE HPV TEST USING HYBRID CAPTUR... QIAGEN GAITHERSBURG, INC P890064 S006 03/17/1999
DIGENE HYBRID CAPTURE II HIGH-RISK HPV DNA TEST QIAGEN GAITHERSBURG, INC P890064 S007 03/16/2000
HCS HPV, HCII HPV QIAGEN GAITHERSBURG, INC P890064 S008 09/12/2000
DIGENE HYBRID CAPTURE 2 (HC2) HIGH-RISK HPV DNA TE... QIAGEN GAITHERSBURG, INC P890064 S009 03/31/2003
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