ClearanceBrief
510(k) K831735 ยท LAS Drug Specific Control Materials

MAPROTILINE

ApplicantUtak Laboratories, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 26, 1983
ReceivedMay 31, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K831735

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.