PW DOPPLER VASCULAR PROBES

PW DOPPLER VASCULAR PROBES is an FDA 510(k)-cleared medical device (K935994) manufactured by Koven Technology, 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 May 10, 1995. Regulation: 8.