ClearanceBrief
510(k) K890522 ยท BZG Spirometer, Diagnostic

PURITAN BENNETT PB900A DIAGNOSTIC SPIROMETER

ApplicantPuritan Bennett Corp., Overland Park KS, US
DecisionSubstantially Equivalent, Apr 21, 1989
ReceivedFeb 2, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K890522

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.