
Medical Devices, Inc.
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BIPOLAR ENDOSTASIS PROBE, BEST (TM) is an FDA 510(k)-cleared medical device (K915408) manufactured by Medical Devices, 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 March 10, 1992. Regulation: 8.