ClearanceBrief
510(k) K923323 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

INTERMITTENT INJECTION SITE

ApplicantKawasumi Laboratories Co., Ltd., Tokyo, JP
DecisionSubstantially Equivalent, Jul 13, 1993
ReceivedJul 7, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K923323

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.