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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 supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameFPSA FLEX REAGENT CARTRIDGE
Classification Nametest,prostate specific antigen,free,(noncomplexed) to distinguish prostate cancer from benign conditions
Generic Nameprostate specific antigen (psa) for detection and management of prostate cancers
ApplicantSIEMENS CORP.
PMA NumberP020027
Supplement NumberS009
Date Received12/02/2008
Decision Date05/17/2010
Product Code
MTG[ Registered Establishments with MTG ]
Advisory Committee Immunology
Supplement Typenormal 180 day track
Supplement Reason change design/components/specifications - component
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for the following changes: 1) detection technology from spectrophotometry to chemiluminesence; 2) appropriate reagent process changes to accommodate chemiluminesence detection; 3) usage on the dimension vista 1500 system; 4) usage on the dimension vista 3000t system which consists of two dimension vista 1500 systems connected by a sample track transport mechanism; and 5) usage on the dimension vista 1500 system connected to the streamlab analytical workcell laboratory automation system. The device, as modified, will be marketed under the trade name dimension vista fpsa flex reagent cartridge and is indicated for: the fpsa method for the dimension vista system is an in vitro diagnostic test intended to quantitatively measure free prostate specific antigen (fpsa) in human serum and plasma. Measurements of fpsa are used in conjunction with total psa (tpsa) method on dimension vista systen to calculate fpsa to tpsa ratio expressed as a percent fpsa. The percent fpsa is used as an aid in distinguishing prostate cancer from benign prostate conditions in men 50 years or older with tpsa of 4. 0 to 1. 0 ng/ml and dre findings not suspicious for cancer. Prostate biopsy is required for diagnosis of cancer.
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