510(k) K861902 ยท HHD Pad, Menstrual, Unscented
KOTEX PROFILE SHAPED MAXI PAD
| Applicant | Kimberly-Clark Corp., Neenah WI, US |
| Decision | Substantially Equivalent, Jun 9, 1986 |
| Received | May 16, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861902
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.