510(k) K040922 ยท DQY Catheter, Percutaneous
VENTURE WIRE CONTROL CATHETER
| Applicant | Velocimed, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Aug 18, 2004 |
| Received | Apr 8, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K040922
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 22, 2017 | Vascular 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 |
DQY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.