ClearanceBrief
510(k) K062340 ยท LYK Angioscope

CARDIOOPTICS AUGMENTATIVE CARDIAC OPTICAL IMAGING SYSTEM

ApplicantCardio-Optics, Inc., Boulder CO, US
DecisionSubstantially Equivalent, Nov 30, 2006
ReceivedAug 10, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K062340

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.