510(k) K801679 ยท FJS Catheter, Peritoneal, Long-Term Indwelling
BETA-CAP II
| Applicant | Quinton, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 3, 1980 |
| Received | Jul 22, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801679
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.