VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger

VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger is an FDA 510(k)-cleared medical device (K212065) manufactured by Remington Medical, 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 October 6, 2021. Regulation: 8.