510(k) K790122 ยท GOK Antisera, Hai (Including Hai Control), Rubella
RUBANON
| Applicant | Organon, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 15, 1979 |
| Received | Jan 23, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790122
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.