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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 PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceRIANEN 3H
Generic NameKIT, ASSAY, ESTROGEN RECEPTOR
Regulation Number864.1860
ApplicantDUPONT LEGAL
4417 LANCASTER PIKE
WILMINGTON, DE 19805
PMA NumberP800061
Supplement NumberS002
Date Received04/09/1982
Decision Date05/21/1982
Withdrawal Date 02/07/2012
Product Code LPJ 
Advisory Committee Clinical Chemistry
Expedited Review Granted? No
Combination ProductNo
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