ClearanceBrief
510(k) K042910 ยท DQY Catheter, Percutaneous

VENTURE WIRE CONTROL CATHETER, MODEL WCC

ApplicantVelocimed, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Nov 22, 2004
ReceivedOct 21, 2004
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K042910

DateFirm and productCodeLinked 510(k)
Mar 7, 2018SPS Sterilization, Inc
Vascular Solutions Venture Rx Catheter, 6F, resterilized.
Terminated
DQYNone listed
May 22, 2017Vascular Solutions, Inc.
Venture RX Catheter, Model 5820; Venture OTW Catheter, Model 5821; Venture CS Catheter, Model 5822. Sterilized using ethylene oxide, Rx Only. The Venture catheter is indicated for directing, stee
Terminated
DQYNone listed

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