510(k) K060897 ยท FJS Catheter, Peritoneal, Long-Term Indwelling
EMBEDDING TOOL, MODEL TE-1000
| Applicant | Medigroup, Inc., Oswego IL, US |
| Decision | Substantially Equivalent, Jul 18, 2006 |
| Received | Apr 3, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060897
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.