510(k) K813472 ยท JJJ Counter (Beta, Gamma) For Clinical Use
LS 5800 SERIES LIQUID SCINTILLATION
| Applicant | Beckman Instruments, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 29, 1981 |
| Received | Dec 14, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813472
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.