510(k) K884379 ยท FGD Catheter, Retention, Barium Enema With Bag
MAGLINTE ENTEROCLYSIS CATHETER
| Applicant | Lafayette Pharmacal, Inc., Lafayette IN, US |
| Decision | Substantially Equivalent, Feb 28, 1989 |
| Received | Oct 18, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884379
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.