510(k) K904840 ยท HIS Condom
ORION PLUS/MODIFICATION
| Applicant | Mayer Laboratories, Oakland CA, US |
| Decision | Substantially Equivalent, Nov 20, 1990 |
| Received | Oct 24, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904840
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.