510(k) K890013 ยท HHT Spatula, Cervical, Cytological
KOTEX SUPER MAXI PADS
| Applicant | Kimberly-Clark Corp., Washington DC, US |
| Decision | Substantially Equivalent, Apr 25, 1989 |
| Received | Jan 3, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890013
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.