ClearanceBrief
510(k) K242757 ยท MCW Catheter, Peripheral, Atherectomy

Rotarex Atherectomy System

ApplicantBard Peripheral Vascular, Inc., Tempe AZ, US
DecisionSubstantially Equivalent, Jan 30, 2025
ReceivedSep 12, 2024
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K242757

DateFirm and productCodeLinked 510(k)
Mar 5, 2025Bard Peripheral Vascular Inc
Rotarex Atherectomy System and Instructions for Use, BD SET Rotarex: S 6 F x 110 cm, REF: 80236; S 6 F x 135 cm, REF: 80237; S 8 F x 85 cm, REF: 80238; S 8 F x 110 cm, REF: 80239
Open, Classified
MCWNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.