ClearanceBrief
510(k) K910142 ยท FPA Set, Administration, Intravascular

SPARK KIT(R), MODIFICATION

ApplicantLyphomed, Inc., Melrose Park IL, US
DecisionUnknown, May 14, 1991
ReceivedJan 14, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910142

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.