ClearanceBrief
510(k) K901454 ยท DTK Filter, Intravascular, Cardiovascular

VENA CAVA FILTER

ApplicantVena-Tech, Inc., Evanston IL, US
DecisionSubstantially Equivalent, May 29, 1991
ReceivedMar 27, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K901454

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.