ClearanceBrief
510(k) K922034 ยท DPW Flowmeter, Blood, Cardiovascular

LV-20 VOLUMETER, 20 MHZ DOPPLER BLOOD FLOW METER

ApplicantTitronics Medical Instruments, Inc., Iowa City IA, US
DecisionSubstantially Equivalent, May 18, 1993
ReceivedMay 1, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K922034

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.