PSG DIRECTIONAL HYDROPHILIC GUIDE WIRE

PSG DIRECTIONAL HYDROPHILIC GUIDE WIRE is an FDA 510(k)-cleared medical device (K931327) manufactured by Peripheral Systems Group. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 13, 1993. Regulation: 8.