MEDI-TECH PLATFORM GUIDE CATHETER

MEDI-TECH PLATFORM GUIDE CATHETER is an FDA 510(k)-cleared medical device (K952345) manufactured by Medi-Tech, 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 August 16, 1995. Regulation: 8.