510(k) K812217 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
FLUORO AUTOMATIC BRIGHTNESS SYS
| Applicant | Keystone X-Ray, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 16, 1981 |
| Received | Aug 5, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812217
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.