ClearanceBrief
510(k) K113833 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

VITAL SIGNS MONITOR

ApplicantGuangdong Biolight Meditech Co., Ltd., Shanghai, CN
DecisionSubstantially Equivalent, May 1, 2012
ReceivedDec 27, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K113833

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.