ClearanceBrief
510(k) K833762 ยท LJE Catheter, Nephrostomy

PERCUTANEOUS RETROGRADE NEPHROSTOMY

ApplicantVpi, Walker MI, US
DecisionSubstantially Equivalent, Feb 10, 1984
ReceivedOct 26, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K833762

DateFirm and productCodeLinked 510(k)
Jan 4, 2019Cook Inc.
Percutaneous Entry Set, Nephrostomy Catheter, Global Product No. G14649
Terminated
LJENone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.