510(k) K131225 ยท DQY Catheter, Percutaneous
ADROIT GUIDING CATHETER
| Applicant | Cordis Corp., A Johnson & Johnson Co., Fremont CA, US |
| Decision | Substantially Equivalent, May 29, 2013 |
| Received | Apr 30, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K131225
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 1, 2013 | Cordis Corporation Cordis ADROIT 6F Guiding Catheter
Product Usage:
For intravascular introduction of interventional and/or diagnostic devices into the coronary or peripheral vascular system. Terminated |
DQY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.