ClearanceBrief
510(k) K896120 ยท BZG Spirometer, Diagnostic

SCHILLER MODEL SP-100 SPIROVIT(TM)

ApplicantSchiller America, Inc., Tustin CA, US
DecisionSubstantially Equivalent, Jan 9, 1990
ReceivedOct 24, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K896120

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.