ClearanceBrief
510(k) K935302 ยท HKS Prism, Gonioscopic

OSHER SURGICAL GONIO/POSTERIOR POLE LENS

ApplicantOcular Instruments, Inc., Bellevue WA, US
DecisionSubstantially Equivalent, Apr 1, 1994
ReceivedNov 2, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K935302

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.