ClearanceBrief
510(k) K893987 ยท LXS Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla

NIDEK MODEL YC-1200

ApplicantNidek, Inc., El Toro CA, US
DecisionSubstantially Equivalent, Aug 18, 1989
ReceivedJun 5, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K893987

DateFirm and productCodeLinked 510(k)
Apr 2, 2015Nidek Inc
YC-1800 OPHTHALMIC YAG LASER SYSTEM; The YC-1800 allows the safe and bloodless treatment of intraocular diseases for outpatients by mechanical disruption caused by energy of the YAG laser pulses.
Terminated
LXSNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.