ClearanceBrief
510(k) K990962 ยท JAX Pneumotachometer

FLOSENSE, MODEL 29-8010

ApplicantSdi Diagnostics, Inc., Easton MA, US
DecisionSubstantially Equivalent, Jan 7, 2000
ReceivedMar 22, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K990962

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.