ClearanceBrief
510(k) K830084 ยท LYK Angioscope

ANGIOSCOPE

ApplicantTrimedyne, Inc., Walker MI, US
DecisionSubstantially Equivalent, Jun 2, 1983
ReceivedJan 11, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830084

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.