ANGIOTEC SPX SPLIT SCREEN DUAL CHANNEL SCAN CONV.

ANGIOTEC SPX SPLIT SCREEN DUAL CHANNEL SCAN CONV. is an FDA 510(k)-cleared medical device (K893476) manufactured by Andros Analyzers, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 22, 1989. Regulation: 8.