510(k) K810716 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
X-RAY IMAGE INTENSIFIER PRODUCTS
| Applicant | Instrumentation Camera, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 23, 1981 |
| Received | Mar 17, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810716
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.