510(k) K980870 ยท EZL Catheter, Retention Type, Balloon
RUSCH SILICONE FOLEY CATHETER
| Applicant | Rusch, Inc., Jeffrey NH, US |
| Decision | Substantially Equivalent, Jun 9, 1998 |
| Received | Mar 4, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980870
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.