MODIFIED EXEL 2400 ELITE/U & EXEL 2400E/U

MODIFIED EXEL 2400 ELITE/U & EXEL 2400E/U is an FDA 510(k)-cleared medical device (K900170) manufactured by Elscint, 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 July 24, 1990. Regulation: 8.