510(k) K971354 ยท FEG Tube, Double Lumen For Intestinal Decompression And/Or Intubation
KNOTT NG TUBE
| Applicant | Michael M. Knott, M.D., Tahoe City CA, US |
| Decision | Substantially Equivalent, Nov 19, 1997 |
| Received | Apr 11, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971354
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.