510(k) K780179 ยท JJJ Counter (Beta, Gamma) For Clinical Use
LIQUID SCINTILLATION COUNTER
| Applicant | Roche Medical Electronics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 23, 1978 |
| Received | Feb 3, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780179
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.