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Mercia Diagnostics , Ltd.

FDA 510(k) & PMA Approved Devices — 17 products

Total Devices17
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K915479 CAPTIA CMV-TALFZ1992-05-04 View
510(k) K904524 CAPTIA(R) SYPHILIS M, MODIFICATIONLIP1990-12-26 View
510(k) K900654 MODIFIED CAPTIA(R) SYPHILIS-MLIP1990-03-08 View
510(k) K896295 CAPTIA(R) CMV-MLFZ1990-03-06 View
510(k) K896194 CAPTIA(R) CMV-GLFZ1990-03-06 View
510(k) K900655 MODIFIED CAPTIA(R) TOXO-MLGD1990-03-06 View
510(k) K885300 CAPTIA(R) RUBELLA-MLFX1989-08-15 View
510(k) K883924 CAPTIA(R) RUBELLA-GLFX1989-08-15 View
510(k) K892802 SUPER DUOJWZ1989-06-13 View
510(k) K881425 CAPTIA(R) SYPHILIS-GLIP1988-08-04 View
510(k) K880918 CAPTIA TOXO-GLGD1988-08-01 View
510(k) K875138 TRICHOMATE(R) SUPERJWZ1988-05-13 View
510(k) K873740 ROTASCREEN EIALIQ1987-11-27 View
510(k) K872568 ROTASCREENGOB1987-09-14 View
510(k) K871548 CAPTIA(R) SYPHILIS-MLIP1987-08-07 View
510(k) K871746 CAPTIA(R) TOXO-M: AN ENZYME IMMUNOASSAYLGD1987-07-31 View
510(k) K863499 CANDIDATE(R) SUPERLRF1987-03-19 View
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