ClearanceBrief
510(k) K820652 ยท

EXHALED HYDROGEN MONITOR

ApplicantKeymed, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 1, 1982
ReceivedMar 9, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820652

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.