TOBRAMYCIN 125I RIA KIT

TOBRAMYCIN 125I RIA KIT is an FDA 510(k)-cleared medical device (K780182) manufactured by New England Nuclear. 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 February 12, 1978. Regulation: 8.