ClearanceBrief
510(k) K960007 ยท MPA Endoilluminator

STORZ MVS 1011A DISPOSABLE FIBEROPTIC ENDOILLUMINATOR

ApplicantStorz, St. Louis MO, US
DecisionSubstantially Equivalent, Mar 26, 1996
ReceivedJan 2, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960007

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.