510(k) K893390 ยท KOD Catheter, Urological
MODIFIED PRISTINE CULTURE CATHETER
| Applicant | Hml Medical, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Sep 7, 1989 |
| Received | May 1, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893390
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.