ClearanceBrief
510(k) K915577 ยท CAR Monitor, Spinal-Fluid Pressure, Electrically Powered

IMPRAFLO POSTOPERATIVE AUTOTRANSFUSION DEVICE

ApplicantImpra, Inc., Tempe AZ, US
DecisionSubstantially Equivalent, Mar 11, 1992
ReceivedDec 13, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K915577

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.