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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 NameRIANEN(TM) (3H) PROGESTIN RECEPTOR ASSAY KIT
Classification Namekit, assay, progesterone receptor
Generic Nameprogestin receptor assay kit
Regulation Number864.1860
ApplicantDUPONT LEGAL
PMA NumberP820052
Date Received08/03/1982
Decision Date08/31/1983
Withdrawal Date 02/07/2012
Product Code
LPI
Notice Date 10/12/1983
Advisory Committee Clinical Chemistry
Expedited Review Granted? No
Combination Product No
Supplements: S001 S002 S003 S004 S005 S006 
S007 S008 
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