ClearanceBrief
510(k) K841618 ยท FZX Guide, Surgical, Instrument

THREADING TUBE

ApplicantPlastafil, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 27, 1984
ReceivedApr 19, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K841618

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.