INTERSPEC 2 MHZ, TRANSCRANIAL PULSED WAVE DOPPLER

INTERSPEC 2 MHZ, TRANSCRANIAL PULSED WAVE DOPPLER is an FDA 510(k)-cleared medical device (K900155) manufactured by Interspec, 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 October 4, 1990. Regulation: 8.