510(k) K874094 ยท JJJ Counter (Beta, Gamma) For Clinical Use
1205 BETAPLATE LIQUID SCINTILLATION COUNTER
| Applicant | Lkb Instruments, Inc., Gaithersburg MD, US |
| Decision | Substantially Equivalent, Nov 4, 1987 |
| Received | Sep 30, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874094
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.