510(k) K161839 ยท OWB Interventional Fluoroscopic X-Ray System
2D Quantitative Analysis
| Applicant | Philips Medical Systems Nederland B.V., Best, NL |
| Decision | Substantially Equivalent, Jul 29, 2016 |
| Received | Jul 5, 2016 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K161839
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.