MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE

MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE is an FDA 510(k)-cleared medical device (K911099) manufactured by Pilling Co.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 24, 1991. Regulation: 8.