510(k) K001578 ยท DQO Catheter, Intravascular, Diagnostic
ANGIODYNAMICS SOFT-VU HYDROPHILIC COATED ANGIOGRAPHIC CATHETER
| Applicant | AngioDynamics, Inc., Queensburgy NY, US |
| Decision | Substantially Equivalent, Oct 13, 2000 |
| Received | May 22, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K001578
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 22, 2016 | Stryker Sustainability Solutions AngioDynamics Soft Vu Omni Flush Angiographic Catheter
Model Number: 10732203 Terminated |
DQO | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.