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M.K. Meditech Co. , Ltd.
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DUOPRO SAFETY SYRINGE (DUOPROSS) is an FDA 510(k)-cleared medical device (K022806) manufactured by M.K. Meditech Co. , Ltd.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 18, 2002. Regulation: 8.

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