Mercia Diagnostics , Ltd.
Mercia Diagnostics , Ltd. holds FDA 510(k) medical device clearances, first cleared 1987, most recent 1992.
Top product codes for Mercia Diagnostics , Ltd.
Recent clearances by Mercia Diagnostics , Ltd.
- K915479 — CAPTIA CMV-TA
- K904524 — CAPTIA(R) SYPHILIS M, MODIFICATION
- K900654 — MODIFIED CAPTIA(R) SYPHILIS-M
- K896194 — CAPTIA(R) CMV-G
- K896295 — CAPTIA(R) CMV-M
- K900655 — MODIFIED CAPTIA(R) TOXO-M
- K883924 — CAPTIA(R) RUBELLA-G
- K885300 — CAPTIA(R) RUBELLA-M
- K892802 — SUPER DUO
- K881425 — CAPTIA(R) SYPHILIS-G
- K880918 — CAPTIA TOXO-G
- K875138 — TRICHOMATE(R) SUPER
- K873740 — ROTASCREEN EIA
- K872568 — ROTASCREEN
- K871548 — CAPTIA(R) SYPHILIS-M
- K871746 — CAPTIA(R) TOXO-M: AN ENZYME IMMUNOASSAY
- K863499 — CANDIDATE(R) SUPER
Data sourced from openFDA. This site is unofficial and independent of the FDA.