
Mr Associates, Inc.
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BIOPSY FORCEPS W/NEEDLE M.R. ASSOC. is an FDA 510(k)-cleared medical device (K800963) manufactured by Mr Associates, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 7, 1980. Regulation: 8.