ClearanceBrief
510(k) K160448 ยท DQY Catheter, Percutaneous

ARTLINE

ApplicantHealth Line International Corporation, Salt Lake City UT, US
DecisionSubstantially Equivalent, Jul 12, 2016
ReceivedFeb 18, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K160448

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.