ClearanceBrief
510(k) K021606 ยท MMX Device, Percutaneous Retrieval

EN-SNARE ENDOVASCULAR SNARE AND CATHETER

ApplicantMedical Device Technologies, Inc., Gainesville FL, US
DecisionSubstantially Equivalent, May 31, 2002
ReceivedMay 16, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K021606

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.