PLASMA THERAPY TUBESET-E100 SERIES

PLASMA THERAPY TUBESET-E100 SERIES is an FDA 510(k)-cleared medical device (K831747) manufactured by Parker Hannifin Corp.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 29, 1983. Regulation: 8.