DISPOSABLE PERFORATORS, JACOBS, HUDSON

DISPOSABLE PERFORATORS, JACOBS, HUDSON is an FDA 510(k)-cleared medical device (K791101) manufactured by Codman & Shurtleff, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 27, 1979. Regulation: 8.