510(k) K926073 ยท FEG Tube, Double Lumen For Intestinal Decompression And/Or Intubation
ULTRAVAC-NG(TM) NASOGASTRIC SUMP SUCTION TUBE
| Applicant | Surgimark, Inc., Yakima WA, US |
| Decision | Substantially Equivalent, May 15, 1995 |
| Received | Dec 1, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926073
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.