ClearanceBrief
510(k) K821776 ยท LJE Catheter, Nephrostomy

SURGITEK PERCUTANEOUS NEPHROST. STENT

ApplicantMedical Engineering Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 10, 1982
ReceivedJun 17, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821776

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.