510(k) K112687

CONNEX(R) VITAL SIGNS MONITOR 6000 SERIES by Welch Allyn, Inc. — Product Code MWI

K112687 is an FDA 510(k) premarket notification submitted by Welch Allyn, Inc. for the device "CONNEX(R) VITAL SIGNS MONITOR 6000 SERIES". The FDA issued a decision of Substantially Equivalent on November 22, 2011. The device falls under product code MWI (Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)), a Class II device regulated under 21 CFR 870.2300. Welch Allyn, Inc. has at least 10 other 510(k) clearances on record.