ClearanceBrief
510(k) K830396 ยท JSS Kit, Identification, Enterobacteriaceae

UREA-PDA DISK

ApplicantRemel Co., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 8, 1983
ReceivedFeb 7, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830396

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.