ClearanceBrief
510(k) K014170 ยท HJK Lens, Contact, Polymethylmethacrylate, Diagnostic

STAURENGHI WIDE FIELD SCANNING LASER LENS

ApplicantOcular Instruments, Inc., Bellevue WA, US
DecisionSubstantially Equivalent, Mar 4, 2002
ReceivedDec 20, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K014170

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.