510(k) K931924

MARKSMAN ARTERIAL BLOOD GAS SYRINGE by Martech Medical Products, Inc. — Product Code JKA

K931924 is an FDA 510(k) premarket notification submitted by Martech Medical Products, Inc. for the device "MARKSMAN ARTERIAL BLOOD GAS SYRINGE". The FDA issued a decision of Substantially Equivalent on August 3, 1993. The device falls under product code JKA (Tubes, Vials, Systems, Serum Separators, Blood Collection), a Class II device regulated under 21 CFR 862.1675. Martech Medical Products, Inc. has at least 10 other 510(k) clearances on record.