510(k) K811295 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
DIGITAL NOISE REDUCER
| Applicant | Philips Medical Systems (Cleveland), Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jun 23, 1981 |
| Received | May 11, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811295
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.