ClearanceBrief
510(k) K913129 ยท LYK Angioscope

ANGIOLAZ ANGIOSCOPE CATHETER

ApplicantAngiolaz, Inc., Rockingham VT, US
DecisionSubstantially Equivalent, Dec 27, 1991
ReceivedJul 16, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K913129

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.