ClearanceBrief
510(k) K823833 ยท LIB Device, General Purpose, Microbiology, Diagnostic

MICRO STIX #011-010-5000 & HOLDER#5100

ApplicantDynatech Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 8, 1983
ReceivedDec 21, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823833

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.