SPACELABS MEDICAL FULL DISCLOSURE SYSTEM, MODEL 91810

SPACELABS MEDICAL FULL DISCLOSURE SYSTEM, MODEL 91810 is an FDA 510(k)-cleared medical device (K063490) 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 March 14, 2007. Regulation: 8.