ClearanceBrief
510(k) K842481 ยท LYK Angioscope

AMERICAN EDWARDS MINI-FLEX ANGIOSCOPE

ApplicantAmerican Edwards Laboratories, Santa Ana CA, US
DecisionSubstantially Equivalent, Oct 18, 1984
ReceivedJun 25, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K842481

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.