510(k) K935781 ยท FEG Tube, Double Lumen For Intestinal Decompression And/Or Intubation
ARGYLE SALEM SUMP TUBE ANTI-REFLUX VALVE INSERTION TRAY
| Applicant | Sherwood Medical Co., St. Louis MO, US |
| Decision | Unknown, Jan 27, 1995 |
| Received | Dec 6, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935781
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.