ClearanceBrief
510(k) K792141 ยท KRA Catheter, Continuous Flush

CONTINUOUS FLUSH DEVICE

ApplicantPharmaseal Div., Baxter Healthcare Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 5, 1979
ReceivedOct 22, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K792141

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.