ClearanceBrief
510(k) K011899 ยท DPW Flowmeter, Blood, Cardiovascular

PF 5050 PRESSURE UNIT, MODEL PF 5050

ApplicantPerimed AB, Jarfalla, SE
DecisionSubstantially Equivalent, Nov 6, 2001
ReceivedJun 18, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K011899

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.