ClearanceBrief
510(k) K834547 ยท LYK Angioscope

ANGIOSCOPY CATHETER

ApplicantAmerican Edwards Laboratories, Walker MI, US
DecisionSubstantially Equivalent, Jun 11, 1984
ReceivedDec 27, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K834547

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.