510(k) K090259 ยท HIS Condom
OKAMOTO ULTRA THIN
| Applicant | Okamoto USA, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Mar 31, 2009 |
| Received | Feb 2, 2009 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K090259
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.