ClearanceBrief
510(k) K912446 ยท DPW Flowmeter, Blood, Cardiovascular

MODIF. LASERFLO BLOOD PERFUSION MONITOR MODEL BPM2

ApplicantVasamedics, LLC, Minneapolis MN, US
DecisionSubstantially Equivalent, Dec 12, 1991
ReceivedJun 3, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912446

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.