
Perimed, Inc.
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PF404/409/410/411/416/418 W/PF319:0/319:1/319:2 is an FDA 510(k)-cleared medical device (K935495) manufactured by Perimed, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 17, 1994. Regulation: 8.