SCIMED 6 FRENCH MICRO-MAX GUIDE CATHETER

SCIMED 6 FRENCH MICRO-MAX GUIDE CATHETER is an FDA 510(k)-cleared medical device (K953909) manufactured by Scimed. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 12, 1995. Regulation: 8.