510(k) K842316 ยท DQY Catheter, Percutaneous
CRITIKON TRIPLE-LUMEN CENTRAL VENOUS
| Applicant | Critikon Company, LLC, Walker MI, US |
| Decision | Substantially Equivalent, Jul 20, 1984 |
| Received | Jun 12, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842316
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.