ClearanceBrief
510(k) K862512 ยท HKS Prism, Gonioscopic

RITCH TRABECULOPLASTY LASER LENS

ApplicantOcular Instruments, Inc., Bellevue WA, US
DecisionSubstantially Equivalent, Jul 11, 1986
ReceivedJul 1, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K862512

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.