ClearanceBrief
510(k) K153135 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

VITAL SIGNS MONITOR

ApplicantGuangdong Biolight Meditech Co., Ltd., Zhuhai,, CN
DecisionSubstantially Equivalent, Feb 25, 2016
ReceivedOct 30, 2015
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K153135

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.