ClearanceBrief
510(k) K904984 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

ADVANCE 418(TM)

ApplicantPeripheral Systems Group, Mountain View CA, US
DecisionSubstantially Equivalent, Apr 12, 1991
ReceivedNov 2, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K904984

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.