COMBO CATH WIRE-GUIDED CYTOLOGY SYSTEM

COMBO CATH WIRE-GUIDED CYTOLOGY SYSTEM is an FDA 510(k)-cleared medical device (K930348) manufactured by Boston Scientific 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 September 2, 1993. Regulation: 8.