ClearanceBrief
510(k) K010372 ยท HQF Laser, Ophthalmic

LIGHTLAS 532 PHOTOCOAGULATOR

ApplicantLightmed Corp., Shulin City, TW
DecisionSubstantially Equivalent, Aug 22, 2001
ReceivedFeb 7, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K010372

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.