ClearanceBrief
510(k) K993921 ยท BZG Spirometer, Diagnostic

NDD MEDICAL TECHNOLOGIES EASYONE SPIROMETER: FRONTLINE MODEL 2000 AND DIAGNOSTIC MODEL 2001

ApplicantNdd Medical Technologies, Chelmsford MA, US
DecisionSubstantially Equivalent, May 23, 2000
ReceivedNov 18, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K993921

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.