510(k) K140138 ยท OWB Interventional Fluoroscopic X-Ray System
HEARTNAVIGATOR RELEASE 2.0
| Applicant | Philips Medical Systems Nederland B.V., Lutz FL, US |
| Decision | Substantially Equivalent, Jun 10, 2014 |
| Received | Jan 22, 2014 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K140138
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.