ClearanceBrief
510(k) K834237 ยท DQX Wire, Guide, Catheter

GRADUATED GUIDE WIRE BOWL 8

ApplicantSterile Design, Inc., Walker MI, US
DecisionSubstantially Equivalent, Feb 4, 1984
ReceivedDec 6, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K834237

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.