
M.P.S. Pharm'L Int'L
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DERRICK SURESHIELD is an FDA 510(k)-cleared medical device (K953712) manufactured by M.P.S. Pharm'L Int'L. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 11, 1995. Regulation: 8.