ClearanceBrief
510(k) K041376 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

C1 SERIES PATIENT MONITOR, MODELS 863051, 863052, 863053, 863054; OPTIONAL PRINTER FOR CI, MODEL M3925A

ApplicantAnalogic Corp., Peabody MA, US
DecisionSubstantially Equivalent, Jul 20, 2004
ReceivedMay 24, 2004
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K041376

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.