ClearanceBrief
510(k) K850509 ยท LNK Laser For Gastro-Urology Use

ND:YAG FIBERLASE 100 MEDICAL LASER SYSTEM

ApplicantLaser Media, Hauppauge NY, US
DecisionSubstantially Equivalent, Apr 8, 1985
ReceivedFeb 8, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K850509

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.