ClearanceBrief
510(k) K936110 ยท BZH Meter, Peak Flow, Spirometry

ASPIRE

ApplicantDura Pharmaceuticals, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Mar 23, 1995
ReceivedDec 23, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K936110

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.