VasoGuard (V10, V8, V6, V4, V2)

VasoGuard (V10, V8, V6, V4, V2) is an FDA 510(k)-cleared medical device (K233976) manufactured by Corvascular Diagnostics, LLC. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 18, 2024. Regulation: 8.