PERIFLUX PF4001 LASER DOPPLER FLOWMETER

PERIFLUX PF4001 LASER DOPPLER FLOWMETER is an FDA 510(k)-cleared medical device (K922368) manufactured by Perimed, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 2, 1993. Regulation: 8.