ClearanceBrief
510(k) K101542 ยท DQY Catheter, Percutaneous

HEADWAY 17 ADVANCED MICROCATHETER

ApplicantMicroVention, Inc., Tistin CA, US
DecisionSubstantially Equivalent, Aug 6, 2010
ReceivedJun 3, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K101542

DateFirm and productCodeLinked 510(k)
Jan 17, 2025MICROVENTION INC.
Microvention, Headway" 17 Advanced Straight Microcatheter with Hydrophilic Coating, REF: MC172150SX-CN, Sterile R, Rx Only, Lot# 0000629846
Open, Classified
DQYNone listed

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