510(k) K772282 ยท FEG Tube, Double Lumen For Intestinal Decompression And/Or Intubation
HODGE TUBE
| Applicant | Mallinckrodt Critical Care, Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 9, 1978 |
| Received | Dec 12, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K772282
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.