510(k) K852299 ยท CFL Radioimmunoassay, Human Growth Hormone
TERUMO SENSIBEAD EIA HGH KIT
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Jul 9, 1985 |
| Received | May 29, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852299
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.