ClearanceBrief
510(k) K842342 ยท

MWI 888 & 666 DOUBLE LUMEN SUBCLAVIAN

ApplicantMed-West, Inc., Mchenry IL, US
DecisionUnknown, Jun 14, 1984
ReceivedJun 14, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K842342

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.