510(k) K780341 ยท JJJ Counter (Beta, Gamma) For Clinical Use
SCINTILLATION, LIQUID, RACKBETA
| Applicant | Lkb Instruments, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 26, 1978 |
| Received | Mar 1, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780341
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.