
Medical Device Technologies, Inc.
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MEDICAL DEVICE TECHNOLOGIES MANUAL BIOPSY NEEDLE is an FDA 510(k)-cleared medical device (K944837) manufactured by Medical Device 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 October 13, 1994. Regulation: 8.