INTERFERENTIAL STIMULATOR MODEL INF 4150/A

INTERFERENTIAL STIMULATOR MODEL INF 4150/A is an FDA 510(k)-cleared medical device (K921441) manufactured by Biomedical Life Systems, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 7, 1992. Regulation: 8.