ClearanceBrief
510(k) K191532 ยท KRD Device, Vascular, For Promoting Embolization

The Caterpillar and Caterpillar Micro Arterial Embolization Devices

ApplicantC.R. Bard, Inc., Enniscorthy, IE
DecisionSubstantially Equivalent, Feb 4, 2020
ReceivedJun 10, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K191532

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.