510(k) K893217 ยท HIS Condom
LATEX PROPHYLACTIC/RUBBER CONTRACEPTIVE
| Applicant | Shinhen Corp., Los Angeles CA, US |
| Decision | Substantially Equivalent, Jan 10, 1990 |
| Received | Apr 27, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893217
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.