510(k) K780063 ยท GOK Antisera, Hai (Including Hai Control), Rubella
RUBENOSTICON
| Applicant | Organon, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 20, 1978 |
| Received | Jan 12, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780063
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.