510(k) K860587 ยท HHD Pad, Menstrual, Unscented
KOTEX OVERNITE
| Applicant | Kimberly-Clark Corp., Neenah WI, US |
| Decision | Substantially Equivalent, Mar 13, 1986 |
| Received | Feb 19, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860587
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.