510(k) K091637 ยท KNT Tubes, Gastrointestinal (And Accessories)
CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900
| Applicant | Corpak Medsystems, Wheeling IL, US |
| Decision | Substantially Equivalent, Sep 29, 2009 |
| Received | Jun 4, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091637
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.