ClearanceBrief
510(k) K011217 ยท DQO Catheter, Intravascular, Diagnostic

CLEAR OR BRAIDED CONTRAST MEDIA INJECTION LINE WITH OR WITHOUT ROTATOR, CATH LAB KIT

ApplicantAbbott Laboratories, Abbott Park IL, US
DecisionSubstantially Equivalent, May 16, 2001
ReceivedApr 20, 2001
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K011217

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.