ClearanceBrief
510(k) K102433 ยท DPW Flowmeter, Blood, Cardiovascular

MOORVMS-PRES PRESSURE CUFF CONTROLLER

ApplicantMoor Instruments, Ltd., Axminster, Devon, GB
DecisionSubstantially Equivalent, Nov 18, 2010
ReceivedAug 26, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K102433

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.