ClearanceBrief
510(k) K830200 ยท LBI Unit, Neonatal Phototherapy

MICROELISA MINIREADER II

ApplicantDynatech Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 16, 1983
ReceivedJan 20, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830200

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.