ClearanceBrief
510(k) K923054 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

WITT BIOMEDICAL SERIES II-EP

ApplicantWitt Biomedical Corporation, Melbourne FL, US
DecisionSubstantially Equivalent, Feb 25, 1993
ReceivedJun 24, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K923054

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.