INTERSON ENDOCAVITY PROBE FOR ATL ULTRASOUND SYST

INTERSON ENDOCAVITY PROBE FOR ATL ULTRASOUND SYST is an FDA 510(k)-cleared medical device (K911117) manufactured by Interson Corp.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 16, 1991. Regulation: 8.