ClearanceBrief
510(k) K863386 ยท KOB Catheter, Suprapubic (And Accessories)

VESICO SUPRAPUBIC BLADDER DRAINAGE & EXCHANGE SETS

ApplicantAngiomed U.S., Inc., Anaheim CA, US
DecisionSubstantially Equivalent, Oct 24, 1986
ReceivedSep 3, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K863386

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.