ClearanceBrief
510(k) K990075 ยท HQF Laser, Ophthalmic

LPULSA SYL-9000 OPHTHALMIC YAG LASER

ApplicantLight-Med(Usa), Inc., Laguna Hills CA, US
DecisionSubstantially Equivalent, Mar 30, 1999
ReceivedJan 11, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K990075

DateFirm and productCodeLinked 510(k)
Dec 17, 2003LightMed USA Inc
Model LightLas 532 Opthalmic Photocoagulator Laser
Terminated
HQFNone listed

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