ClearanceBrief
510(k) K896515 ยท DPW Flowmeter, Blood, Cardiovascular

LASERFLO BLOOD PERFUSION MONITOR, MODEL BPM2

ApplicantTsi, Inc., Findley MN, US
DecisionSubstantially Equivalent, Feb 13, 1990
ReceivedNov 15, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K896515

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.