ClearanceBrief
510(k) K922484 ยท DQO Catheter, Intravascular, Diagnostic

COBE SAMPLING SITE

ApplicantCobe Cardiovascular, Inc., Arvada CO, US
DecisionSubstantially Equivalent, Dec 3, 1992
ReceivedMay 27, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K922484

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.