PATIENT MONITOR MODELS PM-2000A, PM-2000A+, PM-2000A PRO

PATIENT MONITOR MODELS PM-2000A, PM-2000A+, PM-2000A PRO is an FDA 510(k)-cleared medical device (K123048) manufactured by Advanced Instrumentations, 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 January 10, 2013. Regulation: 8.