510(k) K842176 ยท DQY Catheter, Percutaneous
RAAF DUAL LUMEN CATHETER
| Applicant | Quinton, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jul 13, 1984 |
| Received | Jun 8, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842176
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.