BLADDERSCAN BVI 2500

BLADDERSCAN BVI 2500 is an FDA 510(k)-cleared medical device (K915436) manufactured by Diagnostic Ultrasound Corp.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 2, 1992. Regulation: 8.