510(k) K821366 ยท CFL Radioimmunoassay, Human Growth Hormone
TANDEM - HGH KIT
| Applicant | Hybritech, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 10, 1982 |
| Received | May 10, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821366
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.