510(k) K991811 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
CORDIS MAXI DS PTA BALLOON CATHETER
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Jun 15, 1999 |
| Received | May 27, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K991811
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 4, 2019 | Cordis Corporation Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use. Terminated |
LIT | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.