Bunkerhill Abdominal Aortic Quantification (AAQ)

Bunkerhill Abdominal Aortic Quantification (AAQ) is an FDA 510(k)-cleared medical device (K243779) manufactured by BunkerHill Health. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 30, 2025. Regulation: 8.