510(k) K080679 ยท KNT Tubes, Gastrointestinal (And Accessories)
MODIFICATION TO CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900
| Applicant | Viasys Medsystems, Wheeling IL, US |
| Decision | Substantially Equivalent, Jun 27, 2008 |
| Received | Mar 10, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080679
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.