510(k) K040388 ยท FEG Tube, Double Lumen For Intestinal Decompression And/Or Intubation
NEXT GENERATION SALEM SUMP
| Applicant | Kendall, Mansfield MA, US |
| Decision | Substantially Equivalent, May 17, 2004 |
| Received | Feb 17, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K040388
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.