
Surgical Technologies, Inc.
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BIOPSY CUP FORCEPS is an FDA 510(k)-cleared medical device (K930180) manufactured by Surgical Technologies, 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 February 2, 1994. Regulation: 8.