510(k) K982632 ยท DQY Catheter, Percutaneous
ENVOY AND VISTA BRITE TIP
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Aug 18, 1998 |
| Received | Jul 23, 1998 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K982632
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.