
Martech Medical Products, Inc.
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MARKSMAN ARTERIAL BLOOD GAS SYRINGE is an FDA 510(k)-cleared medical device (K931924) manufactured by Martech Medical Products, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 2, 1993. Regulation: 8.