510(k) K782159 ยท JJA Radio-Labeled Iron Method, Iron (Non-Heme)
DIAGNOSTIC KIT, FERRITAB-FE-59
| Applicant | Leeco Diagnostics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 1, 1979 |
| Received | Dec 22, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K782159
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.