ClearanceBrief
510(k) K933208 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered

BARE-FIBER ENDOILLUMINATOR

ApplicantSurgical Technologies, Inc., Chesterfield MO, US
DecisionSubstantially Equivalent, Dec 14, 1993
ReceivedJul 1, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K933208

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.