Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Premarket Approval (PMA)
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | Registration & Listing | Adverse Events | Recalls | PMA | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
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 NameIMMULITE(R) THIRD GENERATION PSA
Classification Nameprostate-specific antigen (psa) for management of prostate cancers
Generic Namepsa test kit
Regulation Number866.6010
ApplicantDIAGNOSTIC PRODUCTS CORP.
PMA NumberP930027
Supplement NumberS001
Date Received10/18/1995
Decision Date07/11/1996
Product Code
LTJ[ Registered Establishments with LTJ ]
Advisory Committee Immunology
Supplement Typenormal 180 day track
Supplement Reason change design/components/specifications - other
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for changing the coat-a-count psa irma from an immunoradiometric test system for the quantitative measurement of prostate specific antigen in human serum to a solid phase, two-site chemiluminescent immunometric assay for use on the immulite autmoated immunoassay analyzer. The device, as modified, will be marketed under the trade name immulite psa.
-
-