ClearanceBrief
510(k) K003577 ยท FST Light, Surgical, Fiberoptic

STERIS DEEPSITE FIBER OPTIC SURGICAL LIGHT

ApplicantSTERIS Corporation, Montgomery AL, US
DecisionSubstantially Equivalent, Jan 29, 2001
ReceivedNov 20, 2000
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K003577

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.