
Omnis Surgical, Inc.
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COHEN-WARNER TESTICULAR BIOPSY TRAY 2N2720 is an FDA 510(k)-cleared medical device (K844993) manufactured by Omnis Surgical, 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 27, 1985. Regulation: 8.