ClearanceBrief
510(k) K827371 ยท

CILCO ASCAN

ApplicantCilco, Inc., Huntington WV, US
DecisionSubstantially Equivalent, Jul 9, 1982
ReceivedMar 29, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K827371

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.