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. |
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Device | RIANEN(TM) (3H) PROGESTIN RECEPTOR ASSAY KIT |
Generic Name | KIT, ASSAY, PROGESTERONE RECEPTOR |
Regulation Number | 864.1860 |
Applicant | DUPONT LEGAL 4417 LANCASTER PIKE WILMINGTON, DE 19805 |
PMA Number | P820052 |
Supplement Number | S002 |
Date Received | 11/29/1983 |
Decision Date | 02/08/1984 |
Withdrawal Date
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02/07/2012 |
Product Code |
LPI |
Advisory Committee |
Clinical Chemistry |
Expedited Review Granted? | No |
Combination Product | No |
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