ClearanceBrief
510(k) K160229 ยท FCG Biopsy Needle

Echotip Ultra Endobronchial High Definition Ultrasound Needle, Echotip Procore Endobronchial High Definition Ultrasound Biopsy Needle

ApplicantCook Ireland, Ltd., Limerick, IE
DecisionSubstantially Equivalent, Mar 21, 2016
ReceivedFeb 1, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K160229

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.