ClearanceBrief
510(k) K033988 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

GOLDWAY UT4000A VITAL SIGNS MONITOR

ApplicantGoldway (Us), Inc., San Marino CA, US
DecisionSubstantially Equivalent, Feb 25, 2004
ReceivedDec 23, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K033988

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.