510(k) K143412 ยท DQY Catheter, Percutaneous
ADROIT Guiding Catheter
| Applicant | Cordis Corporation, Fremont CA, US |
| Decision | Substantially Equivalent, Jan 14, 2015 |
| Received | Nov 28, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K143412
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 7, 2019 | Cordis Corporation Cordis Vista Brite Tip & Androit Guiding Catheters
Product Usage:
The guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or per Terminated |
DQY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.