ClearanceBrief
510(k) K926003 ยท DQO Catheter, Intravascular, Diagnostic

SCHNEIDER SOFTIP SST ANGIOGRAPHIC (DIAG) CATHETER

ApplicantSchneider Intl., Ltd., Plymouth MN, US
DecisionSubstantially Equivalent, Jun 7, 1993
ReceivedNov 27, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K926003

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.