ClearanceBrief
510(k) K033188 ยท MMX Device, Percutaneous Retrieval

TEXAN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050

ApplicantIdev Technologies, Inc., Houston TX, US
DecisionSubstantially Equivalent, Nov 19, 2003
ReceivedOct 1, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K033188

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.