510(k) K852815 ยท DQY Catheter, Percutaneous
TRIPLE LUMEN RIGHT ATRIAL CATHETER
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Aug 26, 1985 |
| Received | Jul 2, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852815
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.