
E.G. Dick & Assoc.
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WILLIAMS-FRITTS PLEURAL BIOPSY NEEDLE is an FDA 510(k)-cleared medical device (K883876) manufactured by E.G. Dick & Assoc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 6, 1988. Regulation: 8.