510(k) K013017 ยท FJS Catheter, Peritoneal, Long-Term Indwelling
MEDIGROUP KEY TUBE
| Applicant | Janin Group, Inc., Naperville IL, US |
| Decision | Substantially Equivalent, Dec 6, 2001 |
| Received | Sep 7, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013017
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.