
Gallini U.S., LLC
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ACRI R NEEDLE is an FDA 510(k)-cleared medical device (K980248) manufactured by Gallini U.S., LLC. 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 February 17, 1998. Regulation: 8.