510(k) K852388 ยท DQY Catheter, Percutaneous
MAHURKAR SUBCLAVIAN CATHETER INSERTION KIT
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Unknown, Aug 22, 1985 |
| Received | Jun 10, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852388
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.