ClearanceBrief
510(k) K953676 ยท MAV Syringe, Balloon Inflation

BREEZE DIGITAL INFLATION DEVICE

ApplicantNamic, Glens Falls NY, US
DecisionSubstantially Equivalent, Mar 29, 1996
ReceivedAug 7, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K953676

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.