ClearanceBrief
510(k) K022276 ยท BZG Spirometer, Diagnostic

KOKOMATE

ApplicantFerraris Respiratory, Inc., Louisville CO, US
DecisionSubstantially Equivalent, Oct 4, 2002
ReceivedJul 15, 2002
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K022276

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.