510(k) K053410 ยท FEG Tube, Double Lumen For Intestinal Decompression And/Or Intubation
GIENTRIPORT WITH UNIVERSAL SINGLE LUMEN ADAPTOR
| Applicant | Kendall, Mansfield MA, US |
| Decision | Substantially Equivalent, Jan 6, 2006 |
| Received | Dec 7, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053410
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.