SNYDER HEMOVAC TM VENTED WOUND KIT

SNYDER HEMOVAC TM VENTED WOUND KIT is an FDA 510(k)-cleared medical device (K800577) manufactured by Snyder Laboratories, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 15, 1980. Regulation: 8.