510(k) K121772 ยท OWB Interventional Fluoroscopic X-Ray System
ALLURA 3D-RA REL 6, 3D ROADMAP REL 1, MR-CT ROADMAP REL 1
| Applicant | Philips Medical Systems Nederland B.V., Best Noord-Brabant, NL |
| Decision | Substantially Equivalent, Mar 21, 2013 |
| Received | Jun 15, 2012 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K121772
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.