ClearanceBrief
510(k) K913395 ยท BZG Spirometer, Diagnostic

EZ-1 SYSTEM RESPIRATORY EFFORT SENSORS

ApplicantPro-Tech, Inc., Woodinville WA, US
DecisionSubstantially Equivalent, May 20, 1992
ReceivedJul 30, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K913395

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.