ClearanceBrief
510(k) K780673 ยท FPK Tubing, Fluid Delivery

CENTRAL CATHETER KIT

ApplicantArgon Medical Corp., Mchenry IL, US
DecisionSubstantially Equivalent, May 16, 1978
ReceivedApr 24, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780673

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.