ClearanceBrief
510(k) K060135 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

MORTARA SURVEYOR TELEMETRY CENTRAL STATION

ApplicantMortara Instrument, Inc., Milwaukee WI, US
DecisionSubstantially Equivalent, May 15, 2006
ReceivedJan 19, 2006
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K060135

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.