UMI AMNIOCENTESIS KIT W/SPINAL NEEDLE

UMI AMNIOCENTESIS KIT W/SPINAL NEEDLE is an FDA 510(k)-cleared medical device (K844558) manufactured by Universal Medical Instrument Corp.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 30, 1985. Regulation: 8.