TELETHERMOGRAPHIC CAMERA, SERIES A, E, S AND P

TELETHERMOGRAPHIC CAMERA, SERIES A, E, S AND P is an FDA 510(k)-cleared medical device (K033967) manufactured by Flir Systems. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 8, 2004. Regulation: 8.