ClearanceBrief
510(k) K133988 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

TEMPUS PRO EXTENDED FEATURES

ApplicantRemote Diagnostic Technologies , Ltd., Hampshire, GB
DecisionSubstantially Equivalent, May 16, 2014
ReceivedDec 26, 2013
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K133988

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.