ClearanceBrief
510(k) K110214 ยท EZL Catheter, Retention Type, Balloon

DIRECTVISION CATHETER, UNCOATED

ApplicantPercuvision, Ashland MA, US
DecisionSubstantially Equivalent, May 27, 2011
ReceivedJan 25, 2011
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K110214

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.