ClearanceBrief
510(k) K911763 ยท DPW Flowmeter, Blood, Cardiovascular

LASERFLO(R) BLOOD PERFUSION MONITOR (MODEL BPM2)

ApplicantVasamedics, LLC, Minneapolis MN, US
DecisionSubstantially Equivalent, Aug 13, 1991
ReceivedApr 19, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K911763

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.