INFRAVIB MASSAGER - MODEL PR-1000

INFRAVIB MASSAGER - MODEL PR-1000 is an FDA 510(k)-cleared medical device (K900384) manufactured by Infralux International, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 26, 1990. Regulation: 8.