ClearanceBrief
510(k) K830571 ยท KYX Dispenser, Liquid Medication

BOTTLE ADAPTER

ApplicantBurron Medical Products, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 24, 1983
ReceivedFeb 23, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830571

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.