510(k) K832784 ยท DQY Catheter, Percutaneous
ULTRA LIGHT RAAF CATHETER
| Applicant | Quinton, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 20, 1983 |
| Received | Aug 16, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832784
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.