ClearanceBrief
510(k) K113112 ยท DQY Catheter, Percutaneous

CLEARWAY RX NB CATHETER

ApplicantAtrium Medical Corp., Hudson NH, US
DecisionSubstantially Equivalent, Nov 17, 2011
ReceivedOct 20, 2011
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K113112

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.