510(k) K905026 ยท FGD Catheter, Retention, Barium Enema With Bag
DUAL FLEX NON-LATEX
| Applicant | Mmi, Inc., Southfield MI, US |
| Decision | Substantially Equivalent, Dec 18, 1991 |
| Received | Nov 7, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905026
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.