
Davol, Inc.
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DAVOL ENDO-FLO SUCT/IRRI PROBE (FOR GEN SURGERY) is an FDA 510(k)-cleared medical device (K914526) manufactured by Davol, Inc.. 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 November 21, 1991. Regulation: 8.