ClearanceBrief
510(k) K143304 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

Sickbay Clinical Platform

ApplicantMedical Informatics Corp, Houston TX, US
DecisionSubstantially Equivalent, May 26, 2015
ReceivedNov 18, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K143304

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.