ClearanceBrief
510(k) K902788 ยท FIB Protector, Transducer, Dialysis

CLEM TM

ApplicantArbo Medical, Inc., Ann Arbor MI, US
DecisionSubstantially Equivalent, Sep 12, 1990
ReceivedJun 26, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K902788

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.