MODELS 4100 AND 4300 MULTITHERAPY

MODELS 4100 AND 4300 MULTITHERAPY is an FDA 510(k)-cleared medical device (K945954) manufactured by Spinalight, 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 January 18, 1995. Regulation: 8.