ClearanceBrief
510(k) K060712 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

VITELCARE C-TURTLE PATIENT MONITORING SYSTEM

ApplicantVisual Telecommunications Network, Inc., Mclean VA, US
DecisionSubstantially Equivalent, Apr 19, 2006
ReceivedMar 16, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K060712

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.