ClearanceBrief
510(k) K902292 ยท BZH Meter, Peak Flow, Spirometry

MODIFIED ASSESS(R) PEAK FLOW METER

ApplicantHealth Products, Inc., Cedar Grove NJ, US
DecisionSubstantially Equivalent, Aug 10, 1990
ReceivedMay 22, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K902292

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.