ClearanceBrief
510(k) K001223 ยท FQP Lamp, Operating-Room

ACULUX, MODEL AX3001, AX3002

ApplicantAculux, Naples FL, US
DecisionSubstantially Equivalent, Jun 23, 2000
ReceivedApr 17, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K001223

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.