510(k) K180485 ยท FJS Catheter, Peritoneal, Long-Term Indwelling
Argyle Peritoneal Dialysis Catheter and Kits, Argyle Presternal Peritoneal Dialysis Catheter and Kits, Argyle Peritoneal Dialysis Accessory Two Part Titanium Luer Adapter, Argyle Adult Peritoneal Dialysis Accessory Titanium Catheter Extender
| Applicant | Covidien, LLC, Mansfield MA, US |
| Decision | Unknown, Jul 27, 2018 |
| Received | Feb 23, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180485
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.