SOPHEIA GENTAMICIN EIA KIT

SOPHEIA GENTAMICIN EIA KIT is an FDA 510(k)-cleared medical device (K823387) manufactured by Diagnostic Products Corp.. This device is classified under the Clinical Toxicology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 21, 1982. Regulation: 8.