510(k) K946282 ยท EZC Catheter, Coude
UNIVERSAL URETHRAL CATHETER
| Applicant | Louisville Laboratories, Inc., Louisville KY, US |
| Decision | Substantially Equivalent, Mar 31, 1995 |
| Received | Dec 27, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K946282
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.