510(k) K965211 ยท DQY Catheter, Percutaneous
VISTA BRITE TIP CATHETERS
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Mar 11, 1997 |
| Received | Dec 27, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K965211
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.