510(k) K001136 ยท DQY Catheter, Percutaneous
CORDIS INTRODUCER GUIDE
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Apr 28, 2000 |
| Received | Apr 10, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K001136
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 10, 2005 | Cordis Corporation Vistabritetip IG Introducer, Introducer Guide. Labeled as sterile, sterilized with ethylene oxide gas. For single use only. Catalog number 4038553S Terminated |
DQY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.