ClearanceBrief
510(k) K861648 ยท HJK Lens, Contact, Polymethylmethacrylate, Diagnostic

WISE IRIDOTOMY-SPINCTEROTOMY LENS

ApplicantOcular Instruments, Inc., Bellevue WA, US
DecisionSubstantially Equivalent, Jun 19, 1986
ReceivedApr 30, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K861648

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.