ClearanceBrief
510(k) K920844 ยท DPW Flowmeter, Blood, Cardiovascular

PIM 1.0 LASER DOPPLER PERFUSION IMAGER

ApplicantLisca Development AB, Linkoping, SE
DecisionSubstantially Equivalent, Jul 21, 1992
ReceivedFeb 24, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920844

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.