ClearanceBrief
510(k) K781772 ยท GBA Catheter, Balloon Type

CATHETER, TRANSLUMINAL BALLOON

ApplicantMedi-Tech, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 6, 1979
ReceivedOct 16, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781772

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.