510(k) K770094 ยท EAM Screen, Intensifying, Radiographic
FLUORICON 500 IMAGE INTENSIFIERS
| Applicant | General Electric Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 21, 1977 |
| Received | Jan 17, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770094
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.