
Stryker Corporation
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SERFAS 90-S Electrosurgical Probe is an FDA 510(k)-cleared medical device (K160050) manufactured by Stryker Corporation. 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 May 2, 2016. Regulation: 8.