510(k) K904453 ยท HIS Condom
LABELLING MODIFICATION TO MAXX PLUS
| Applicant | Mayer Laboratories, Oakland CA, US |
| Decision | Substantially Equivalent, Nov 23, 1990 |
| Received | Sep 27, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904453
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.