MODIFICATION TO DEVICE LINK SYSTEM, MODEL M2376A

MODIFICATION TO DEVICE LINK SYSTEM, MODEL M2376A is an FDA 510(k)-cleared medical device (K012094) manufactured by Agilent Technologies, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 19, 2001. Regulation: 8.