
Utah Medical Products, Inc.
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LIBERTY PLUS SYSTEM(PFS-300)/VAGINAL PROBE, LIBERTY PLUS(PFS-044) is an FDA 510(k)-cleared medical device (K970077) manufactured by Utah Medical Products, 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 May 22, 1997. Regulation: 8.