510(k) K172307 ยท OWB Interventional Fluoroscopic X-Ray System
Dynamic Coronary Roadmap 2.0
| Applicant | Philips Medical Systems Nederland B.V., Best Noord-Brabant, NL |
| Decision | Substantially Equivalent, Oct 24, 2017 |
| Received | Jul 31, 2017 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K172307
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.