510(k) K160857 ยท KPR System, X-Ray, Stationary
HF 718BD X-Ray System
| Applicant | Arquilla, Inc. Dba X-Cel X-Ray Corporation, Crystal Lake IL, US |
| Decision | Substantially Equivalent, Feb 24, 2017 |
| Received | Mar 29, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160857
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.