510(k) K875111 ยท HIS Condom
RUBBER CONTRACEPTIVE, LATEX CONDOMS
| Applicant | Okamoto USA, Inc., Stratford CT, US |
| Decision | Substantially Equivalent, Feb 26, 1988 |
| Received | Dec 14, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K875111
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.