ClearanceBrief
510(k) K820125 ยท

COBE CENTRY 2000 RX

ApplicantCobe Laboratories, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 23, 1982
ReceivedJan 18, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820125

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.