
Bio-Vascular, Inc.
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PERI-STRIPS-SLEEVE, PERI-STRIPS-STRIP AND PERI-STRIPS DRY (NON-NAOH-TREATED AND NAOH-TREATED is an FDA 510(k)-cleared medical device (K992537) manufactured by Bio-Vascular, 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 February 21, 2000. Regulation: 8.