ClearanceBrief
510(k) K992104 ยท FPA Set, Administration, Intravascular

PARSET, MODEL A10001E

ApplicantRd Medical Mfg., Inc., Cuelbra PR, US
DecisionSubstantially Equivalent, Aug 23, 1999
ReceivedJun 22, 1999
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K992104

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.