SPACELABS MEDICAL EXPANSION MODULE (MODEL 90352)

SPACELABS MEDICAL EXPANSION MODULE (MODEL 90352) is an FDA 510(k)-cleared medical device (K945429) manufactured by Spacelabs Medical, 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 August 14, 1995. Regulation: 8.