ClearanceBrief
510(k) K073094 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

VITALLINK3 MOBILE VITAL SIGNS SYSTEM

ApplicantTelemedic Systems, Ltd., Taunton, Somerset, GB
DecisionSubstantially Equivalent, Jan 4, 2008
ReceivedNov 1, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K073094

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.