ClearanceBrief
510(k) K031409 ยท GBM Catheter, Urethral

URINARY CATHETERS

ApplicantPromedic, Inc., Mccordsville IN, US
DecisionSubstantially Equivalent, Jun 17, 2003
ReceivedMay 5, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K031409

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.