ClearanceBrief
510(k) K830226 ยท LJE Catheter, Nephrostomy

SURGITEK PERCUTANEOUS NEPHROSTOMY CATH

ApplicantMedical Engineering Corp., Walker MI, US
DecisionSubstantially Equivalent, Feb 9, 1983
ReceivedJan 24, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830226

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.