ClearanceBrief
510(k) K803002 ยท DQR Cannula, Catheter

ELECATH FLUID-DRAIN ASSEMBLY

ApplicantElectro-Catheter Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 22, 1980
ReceivedNov 25, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K803002

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.