ClearanceBrief
510(k) K170322 ยท OOE Ophthalmic Femtosecond Laser

Catalys Precision Laser System

ApplicantAbbott Medical Optics, Inc., Milpitas CA, US
DecisionSubstantially Equivalent, May 19, 2017
ReceivedFeb 1, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K170322

DateFirm and productCodeLinked 510(k)
May 9, 2018Johnson & Johnson Surgical Vision Inc
OptiMedica Catalys Precision Laser System, CE 0044 containing software cOS 5.00.33 Product Label for Serial Numbers: 44109015; 44106215; 44107315; and 44065613 label states "Manufactured for: OptiMe
Terminated
OOENone listed

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