
Pathway Medical Technologies, Inc.
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JETSTREAM G2 NXT SYSTEM, MODEL PV20300 is an FDA 510(k)-cleared medical device (K091509) manufactured by Pathway Medical Technologies, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 18, 2009. Regulation: 8.