ClearanceBrief
510(k) K980192 ยท LJE Catheter, Nephrostomy

MANAN NEPHROSTOMY DRAINAGE CATHETER

ApplicantMedical Device Technologies, Inc., Gainsville FL, US
DecisionSubstantially Equivalent, May 27, 1998
ReceivedJan 20, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K980192

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.