ClearanceBrief
510(k) K020004 ยท BZG Spirometer, Diagnostic

CLINDATALINK VERSION 1.0 FOR SPIROMETRY

ApplicantCompleware Corp., Iowa City IA, US
DecisionSubstantially Equivalent, Jul 24, 2002
ReceivedJan 2, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K020004

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.