510(k) K771048 ยท FEG Tube, Double Lumen For Intestinal Decompression And/Or Intubation
CATHETERS, DRAINAGE
| Applicant | Axiom Medical, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 19, 1977 |
| Received | Jun 10, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K771048
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.