ClearanceBrief
510(k) K910822 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

BARD PERIPHERAL BALLOON DILATATION CATHETER

ApplicantC.R. Bard, Inc., Murray Hill NJ, US
DecisionSubstantially Equivalent, Aug 29, 1991
ReceivedFeb 26, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910822

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.