AIS100 AUTOMATIC INTRAMUSCULAR STIMULATOR

AIS100 AUTOMATIC INTRAMUSCULAR STIMULATOR is an FDA 510(k)-cleared medical device (K040580) manufactured by D.Y. Instrument, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 25, 2004. Regulation: 8.