ClearanceBrief
510(k) K896741 ยท DQO Catheter, Intravascular, Diagnostic

SCHNEIDER MONORAIL-PMC PRESSURE MONITORING CATH.

ApplicantSchneider Intl., Ltd., Minneapolis MN, US
DecisionSubstantially Equivalent, Feb 28, 1990
ReceivedNov 30, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K896741

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.