510(k) K132314 ยท FEG Tube, Double Lumen For Intestinal Decompression And/Or Intubation
MEDLINE ANTI-REFLUX VALVE
| Applicant | Medline Industries, Inc., Mundelein IL, US |
| Decision | Substantially Equivalent, Sep 18, 2013 |
| Received | Jul 25, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132314
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.