ClearanceBrief
510(k) K880890 ยท FYD Apparatus, Exhaust, Surgical

THE S.A.F.E. SYSTEM

ApplicantPfizer Laser Systems, Irvine CA, US
DecisionSubstantially Equivalent, May 11, 1988
ReceivedMar 2, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880890

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.