
Technicon Instruments Corp.
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TECHNICON RA SYSTEMS/TOBRAMYCIN & GENTAMICIN is an FDA 510(k)-cleared medical device (K860868) manufactured by Technicon Instruments 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 April 2, 1986. Regulation: 8.