510(k) K090590 ยท OWB Interventional Fluoroscopic X-Ray System
VERADIUS, MODEL 718-130
| Applicant | Philips Medical Systems North America Co., Bothell WA, US |
| Decision | Substantially Equivalent, Mar 16, 2009 |
| Received | Mar 4, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090590
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.