QAD-1 ANGIO DYNOGRAPH ULTRASO W/5.0 7.5 MHZ PROBES

QAD-1 ANGIO DYNOGRAPH ULTRASO W/5.0 7.5 MHZ PROBES is an FDA 510(k)-cleared medical device (K853217) manufactured by Quantum Medical Systems, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 29, 1985. Regulation: 8.