510(k) K112082 ยท DQY Catheter, Percutaneous
GUIDELINER V2 CATHETER
| Applicant | Vascular Solutions, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Dec 1, 2011 |
| Received | Jul 21, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K112082
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 24, 2012 | Vascular Solutions, Inc. Vascular Solutions, GuideLiner V2 Catheter, Rx only, Sterile EO, Catalog Number 5571, 6F, Vascular Solutions, Inc., 6464 Sycamore Court, Minneapolis, MN 55369.
Intended to be used in conjunction wit Terminated |
DQY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.