Device Recall PSA ELISA Kit

  • Model / Serial
    Catalog number: BC-1019;  RN-34301 05-2010 RN-34353 05-2010 RN-34657 07-2010  RN-34877 07-2010 RN-35018 08-2010 RN-35057 08-2010  RN-35485 09-2010 RN-35699 10-2010 RN-35975 11-2010  RN-35976 11-2010 RN-36412 12-2010 RN-36523 12-2010  RN-36606 01-2011 RN-36821 02-2011 RN-37060 02-2011  RN-37370 03-2011 RN-37371 03-2011 RN-37603 02-2011  RN-37639 04-2011 RN-37645 04-2011 RN-37774 05-2011 RN-38040 06-2011 RN-38155 06-2011 RN-38178 07-2011  RN-38247 07-2011 RN-38913 08-2011 RN-39190 08-2011  RN-39219 08-2011 RN-39250 09-2011 RN-39529 10-2011  RN-39703 11-2011 RN-39833 11-2011 RN-39960 12-2011  RN-39963 12-2011 RN-40108 12-2011 RN-40109 12-2011  RN-40261 12-2011 RN-40340 02-2012 RN-40435 02-2012  RN-40585 03-2012 RN-40586 03-2012 RN-40791 03-2012 RN-40909 03-2012 RN-40915 03-2012 RN-41193 05-2012  RN-41293 05-2012
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide distribution.
  • Product Description
    PSA ELISA Kit. || BioCheck, Foster City, CA 9440. || Quantitative determination of AFP concentration in human serum.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    BioCheck Inc, 323 Vintage Park Dr, Foster City CA 94404-1186
  • Manufacturer Parent Company (2017)
  • Source
    USFDA