ClearanceBrief
510(k) K981326 ยท DQX Wire, Guide, Catheter

LAKE REGION MANUFACTURING GUIDEWIRES

ApplicantLake Region Mfg., Inc., Chaska MN, US
DecisionSubstantially Equivalent, Jul 10, 1998
ReceivedApr 13, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K981326

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.