510(k) K833308 ยท KOC Accessories, Blood Circuit, Hemodialysis
DUAL LUMEN NEEDLE
| Applicant | Quinton, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Dec 27, 1983 |
| Received | Sep 26, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833308
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.