ClearanceBrief
510(k) K896300 ยท BZG Spirometer, Diagnostic

LDW SPIROMETRY SYSTEM

ApplicantLanpher Diagnostic Workstations, Inc., Atherton CA, US
DecisionSubstantially Equivalent, Apr 3, 1990
ReceivedOct 30, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K896300

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.