ClearanceBrief
510(k) K883433 ยท GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered

AMBU TWIN PUMP - (MANUAL SUCTION PUMP)

ApplicantAmbu, Inc., Hanover MD, US
DecisionSubstantially Equivalent, Sep 2, 1988
ReceivedAug 15, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883433

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.