510(k) K853860 ยท DQY Catheter, Percutaneous
REPAIR KIT QUINTON TRIPLE LUMEN RIGHT ATRIAL CATHE
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Oct 18, 1985 |
| Received | Sep 17, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K853860
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.