ClearanceBrief
510(k) K123400 ยท BWF Spirometer, Therapeutic (Incentive)

AEROBIKA POSITIVE EXPIRATORY PRESSURE DEVICE

ApplicantTrudell Medical Intl., London, CA
DecisionSubstantially Equivalent, May 16, 2013
ReceivedNov 5, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K123400

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.