
Diasol, Inc.
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SHELLY PROTECTED AV FISTULA NEEDLE is an FDA 510(k)-cleared medical device (K992653) manufactured by Diasol, 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 October 26, 1999. Regulation: 8.