ClearanceBrief
510(k) K802025 ยท GBA Catheter, Balloon Type

BALLOON RETENTION CHEST CATHETER

ApplicantLoseff Medical Designers, Ltd., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 26, 1980
ReceivedAug 20, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802025

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.