ClearanceBrief
510(k) K052059 ยท MQF Catheter, Assisted Reproduction

IUI CATHETER, MODEL 9057

ApplicantInntec, Inc., Stoughton WI, US
DecisionSubstantially Equivalent, Nov 22, 2005
ReceivedJul 29, 2005
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K052059

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.