
Lazarus Effect, Inc.
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FUNNEL GUIDE CATHETER MODEL G1020608 is an FDA 510(k)-cleared medical device (K102439) manufactured by Lazarus Effect, 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 January 11, 2012. Regulation: 8.