ClearanceBrief
510(k) K952894 ยท HQF Laser, Ophthalmic

VISULINK 900 ARGON

ApplicantCarl Zeiss, Inc., Thornwood NY, US
DecisionSubstantially Equivalent, Aug 14, 1995
ReceivedJun 23, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K952894

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.