
Karl M. Block Co.
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KEITH-A.R.V. is an FDA 510(k)-cleared medical device (K851444) manufactured by Karl M. Block Co.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 9, 1985. Regulation: 8.