510(k) K931156 ยท EXJ Device, Incontinence, Urosheath Type, Sterile
CONE CATH
| Applicant | Sierra Laboratories, Inc., Tucson AZ, US |
| Decision | Substantially Equivalent, Jul 1, 1993 |
| Received | Mar 9, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931156
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.