510(k) K962830 ยท DQY Catheter, Percutaneous
VISTA BRITE TIP CATHETERS
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Oct 17, 1996 |
| Received | Jul 22, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962830
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.