LOUISVILLE CLAMP PRODUCT #65-172

LOUISVILLE CLAMP PRODUCT #65-172 is an FDA 510(k)-cleared medical device (K770503) manufactured by Edward Weck, 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 March 29, 1977. Regulation: 8.