510(k) K844889 ยท GBP Catheter, Multiple Lumen
MENSINK-GOOSEN CATHETER
| Applicant | Goosen Enterprises, Inc., Goldenrod FL, US |
| Decision | Substantially Equivalent, Mar 18, 1985 |
| Received | Dec 17, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844889
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.