ClearanceBrief
510(k) K050541 ยท HQF Laser, Ophthalmic

OMNIGUIDE BEAMPATH CO2 MARK I LASER BEAM DELIVERY

ApplicantOmniguide Communications, Inc., Cambridge MA, US
DecisionSubstantially Equivalent, May 9, 2005
ReceivedMar 2, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K050541

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.