
Technicon Instruments Corp.
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TECHNICON RA SYSTEMS TOBRAMYCIN TEST METHOD is an FDA 510(k)-cleared medical device (K893913) 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 August 20, 1989. Regulation: 8.